United States, et al. v. Stericycle, Inc., et al.; Proposed Final Judgment and Competitive Impact Statement, 5120-5132 [2010-1959]
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Federal Register / Vol. 75, No. 20 / Monday, February 1, 2010 / Notices
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proposed collection of information,
including the validity of the
methodology and assumptions used;
—Enhance the quality, utility, and
clarity of the information to be
collected; and
—Minimize the burden of the collection
of information on those who are to
respond, including through the use of
appropriate automated, electronic,
mechanical, or other technological
collection techniques or other forms
of information technology, e.g.,
permitting electronic submission of
responses.
Overview of This Information
Collection
(1) Type of Information Collection:
Extension of a Currently Approved
Collection.
(2) Title of the Form/Collection:
Release and Receipt of Imported
Firearms, Ammunition and Implements
of War.
(3) Agency form number, if any, and
the applicable component of the
Department of Justice sponsoring the
collection: Form Number: ATF F 6A
(5330.3C). Bureau of Alcohol, Tobacco,
Firearms and Explosives.
(4) Affected public who will be asked
or required to respond, as well as a brief
abstract: Primary: Individuals or
households. Other: Business or other
for-profit, Not-for-profit institutions.
Abstract: The data provided by this
information collection request is used
by ATF to determine if articles imported
meet the statutory and regulatory
criteria for importation and if the
articles shown on the permit application
have been actually imported.
(5) An estimate of the total number of
respondents and the amount of time
estimated for an average respondent to
respond: There will be an estimated
20,000 respondents, who will complete
the form within approximately 24
minutes.
(6) An estimate of the total burden (in
hours) associated with the collection:
There are an estimated 8,000 total
burden hours associated with this
collection.
If additional information is required
contact: Lynn Bryant, Department
Clearance Officer, United States
Department of Justice, Policy and
Planning Staff, Justice Management
Division, Suite 1600, Patrick Henry
Building, 601 D Street, NW.,
Washington, DC 20530.
Dated: January 26, 2010.
Lynn Bryant,
Department Clearance Officer, PRA, United
States Department of Justice.
[FR Doc. 2010–1869 Filed 1–29–10; 8:45 am]
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DEPARTMENT OF JUSTICE
Bureau of Alcohol, Tobacco, Firearms,
and Explosives
[OMB Number 1140–0087]
Agency Information Collection
Activities: Proposed Collection;
Comments Requested
ACTION: 30-Day notice of information
collection under review: eForm 6 access
request.
The Department of Justice (DOJ),
Bureau of Alcohol, Tobacco, Firearms,
and Explosives (ATF) will be submitting
the following information collection
request to the Office of Management and
Budget (OMB) for review and approval
in accordance with the Paperwork
Reduction Act of 1995. The proposed
information collection is published to
obtain comments from the public and
affected agencies. This proposed
information collection was previously
published in the Federal Register
Volume 74, Number 228, page 62597 on
November 30, 2009, allowing for a 60day comment period.
The purpose of this notice is to allow
for an additional 30 days for public
comment until March 3, 2010. This
process is conducted in accordance with
5 CFR 1320.10.
Written comments and/or suggestions
regarding the items contained in this
notice, especially the estimated public
burden and associated response time,
should be directed to The Office of
Management and Budget, Office of
Information and Regulatory Affairs,
Attention Department of Justice Desk
Officer, Washington, DC 20503.
Additionally, comments may be
submitted to OMB via facsimile to (202)
395–5806.
Written comments and suggestions
from the public and affected agencies
concerning the proposed collection of
information are encouraged. Your
comments should address one or more
of the following four points:
—Evaluate whether the proposed
collection of information is necessary
for the proper performance of the
functions of the agency, including
whether the information will have
practical utility;
—Evaluate the accuracy of the agencies
estimate of the burden of the
proposed collection of information,
including the validity of the
methodology and assumptions used;
—Enhance the quality, utility, and
clarity of the information to be
collected; and
—Minimize the burden of the collection
of information on those who are to
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respond, including through the use of
appropriate automated, electronic,
mechanical, or other technological
collection techniques or other forms
of information technology, e.g.,
permitting electronic submission of
responses.
Overview of This Information
Collection
(1) Type of Information Collection:
Extension of a currently approved
collection.
(2) Title of the Form/Collection:
eForm 6 Access Request.
(3) Agency form number, if any, and
the applicable component of the
Department of Justice sponsoring the
collection: Form Number: ATF F 5013.3.
Bureau of Alcohol, Tobacco, Firearms
and Explosives.
(4) Affected public who will be asked
or required to respond, as well as a brief
abstract: Primary: Business or other forprofit. Other: none. Abstract:
Respondents must complete the eForm
6 Access Request form in order to
receive a user ID and password to obtain
access to ATF’s eForm 6 System. The
information is used by the Government
to verify the identity of the end users
prior to issuing passwords.
(5) An estimate of the total number of
respondents and the amount of time
estimated for an average respondent to
respond: There will be an estimated 500
respondents, who will complete the
form within approximately 18 minutes.
(6) An estimate of the total burden (in
hours) associated with the collection:
There are an estimated 150 total burden
hours associated with this collection.
If additional information is required
contact: Lynn Bryant, Department
Clearance Officer, United States
Department of Justice, Policy and
Planning Staff, Justice Management
Division, Suite 1600, Patrick Henry
Building, 601 D Street, NW.,
Washington, DC 20530.
Dated: January 26, 2010.
Lynn Bryant,
Department Clearance Officer, PRA, United
States Department of Justice.
[FR Doc. 2010–1868 Filed 1–29–10; 8:45 am]
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DEPARTMENT OF JUSTICE
Antitrust Division
United States, et al. v. Stericycle, Inc.,
et al.; Proposed Final Judgment and
Competitive Impact Statement
Notice is hereby given pursuant to the
Antitrust Procedures and Penalties Act,
15 U.S.C. 16(b)–(h), that a proposed
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Final Judgment and Competitive Impact
Statement have been filed with the
United States District Court for the
District of Columbia in United States, et
al. v. Stericycle, Inc., et al., Civil Action
No. 1:09–cv–02268. On November 30,
2009, the United States and the States
of Missouri and Nebraska filed a
Complaint alleging that the proposed
acquisition by Stericycle, Inc. of
MedServe, Inc. would violate Section 7
of the Clayton Act, 15 U.S.C. 18. The
proposed Final Judgment, filed the same
time as the Complaint, requires
Stericycle to divest all MedServe assets
used in the provision of infectious waste
collection and treatment services for
Large Quantity Generator (‘‘LQG’’)
customers in the states of Kansas,
Missouri, Nebraska, and Oklahoma.
These assets include an autoclave in
Newton, Kansas; transfer stations in
Kansas City, Kansas; Oklahoma City,
Oklahoma; Omaha, Nebraska; and
Booneville, Missouri; LQG customer
contracts associated with these
facilities; and certain tangible and
intangible assets. Copies of the
Complaint, proposed Final Judgment,
and Competitive Impact Statement are
available for inspection at the
Department of Justice, Antitrust
Division, Antitrust Documents Group,
450 Fifth Street, NW., Suite 1010,
Washington, DC 20530 (telephone: 202–
514–2481), on the Department of
Justice’s Web site at https://
www.usdoj.gov/atr, and at the Office of
the Clerk of the United States District
Court for the District of Columbia.
Copies of these materials may be
obtained from the Antitrust Division
UNITED STATES OF AMERICA, Department of Justice, Antitrust Division, 450 5th
Street, NW., Suite 8700, Washington, DC 20530; STATE OF MISSOURI, Office of
the Attorney General, P.O. Box 899, Jefferson City, Missouri 65102; and STATE OF
NEBRASKA, Office of the Attorney General, 2115 State Capitol Building, Lincoln,
Nebraska 68509–8920, Plaintiffs, v. STERICYCLE, INC., 28161 North Keith Drive,
Lake Forest, Illinois 60045; ATMW ACQUISITION CORP., 28161 North Keith Drive,
Lake Forest, Illinois 60045; MEDSERVE, INC., 6575 West Loop South, Suite 145,
Bellaire, Texas, 77401; and AVISTA CAPITAL PARTNERS, L.P., 6575 West Loop
South, Suite 145, Bellaire, Texas 77401, Defendants.
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Complaint
Plaintiff, the United States of America
(‘‘United States’’), acting under the
direction of the Attorney General of the
United States, and plaintiffs, the State of
Missouri and the State of Nebraska,
acting under the direction of their
respective Attorneys General, bring this
civil antitrust action against defendants,
Stericycle, Inc. and ATMW Acquisition
Corp. and MedServe, Inc. and Avista
Capital Partners, L.P. to enjoin
Stericycle’s proposed acquisition of
MedServe and to obtain other equitable
relief. Plaintiffs complain and allege as
follows:
I. Nature of the Action
1. Pursuant to an agreement and plan
of merger dated May 9, 2009, Stericycle
intends to acquire all of the voting
shares of MedServe in a transaction
valued at $185 million. Defendants
Stericycle and MedServe currently
compete in the provision of infectious
waste collection and treatment services
for large quantity generator (‘‘LQG’’)
customers. The resulting combination
would create a monopoly in the
provision of infectious waste collection
and treatment services for LQG
customers in the states of Missouri,
Nebraska, Oklahoma, and Kansas.
2. The United States, the State of
Missouri, and the State of Nebraska
bring this action to prevent the
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upon request and payment of a copying
fee set by Department of Justice
regulations.
Public comment is invited within 60
days of the date of this notice. Such
comments, and responses thereto, will
be published in the Federal Register
and filed with the Court. Comments
should be directed to Maribeth Petrizzi,
Chief, Litigation II Section, Antitrust
Division, U.S. Department of Justice,
450 Fifth Street, NW., Suite 8700,
Washington, DC 20530 (telephone: 202–
307–0924).
J. Robert Kramer II,
Director of Operations and Civil Enforcement.
United States District Court for the
District of Columbia
CASE NO.: 1:09–cv–02268; JUDGE: John D. Bates;
DECK TYPE: Antitrust; DATE STAMP: November 30,
2009.
proposed acquisition because it would
substantially lessen competition in the
provision of infectious waste collection
and treatment services for LQG
customers in the states of Kansas,
Missouri, Nebraska, and Oklahoma, in
violation of Section 7 of the Clayton
Act, 15 U.S.C. 18.
15 U.S.C. 22, and 28 U.S.C. 1331 and
1337.
5. Defendants transact business, and
have consented to venue and personal
jurisdiction, in the District of Columbia.
Venue is therefore proper in this District
under Section 12 of the Clayton Act, 15
U.S.C. 22 and 28 U.S.C. 1391(c).
II. Jurisdiction and Venue
III. The Defendants
3. The United States brings this action
under Section 15 of the Clayton Act, as
amended, 15 U.S.C. 4 and 25, to prevent
and restrain defendants from violating
Section 7 of the Clayton Act, 15 U.S.C.
18. The State of Missouri and the State
of Nebraska bring this action under
Section 16 of the Clayton Act, 15 U.S.C.
26, to prevent and restrain defendants
from violating Section 7 of the Clayton
Act, 15 U.S.C. 18. The State of Missouri
and the State of Nebraska, by and
through their respective Attorneys
General, or other authorized officials,
bring this action in their sovereign
capacities and as parens patriae on
behalf of the citizens, general welfare,
and economy of each of their states.
4. Defendants collect and treat
infectious waste generated by LQG
customers in the flow of interstate
commerce. Defendants’ activities in
collecting and treating infectious waste
substantially affect interstate commerce.
The Court has jurisdiction over this
action and over the parties pursuant to
6. Defendant Stericycle, Inc. is a
Delaware corporation with its principal
place of business in Lake Forest,
Illinois. Stericycle, a multi-national
company, is the largest provider of
infectious waste collection and
treatment services in the United States,
with operations in nearly all of the
contiguous 48 states, including 46
treatment facilities and 80 transfer and
collection sites. In 2008, Stericycle
reported total worldwide sales of
approximately $1.1 billion, of which
approximately 78 percent were
generated in the United States. ATMW
Acquisition Corp. is a corporation
formed by Stericycle to facilitate its
acquisition of MedServe. Stericycle and
ATMW hereinafter are collectively
referred to as Stericycle.
7. Defendant MedServe is a Delaware
corporation with its principal place of
business in Bellaire, Texas. MedServe is
the second-largest provider of infectious
waste collection and treatment services
in the United States, with operations in
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25 states that include eight treatment
facilities and 18 transfer and collection
sites. In 2008, MedServe had total
revenues of about $35.6 million. Avista
Capital Partners, L.P. is an entity formed
by MedServe to facilitate the acquisition
of MedServe by Stericycle. MedServe
and Avista hereinafter are collectively
referred to as MedServe.
IV. Trade and Commerce
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A. The Relevant Service Market
8. Regulated medical waste is waste
generated in the diagnosis, treatment, or
immunization of human beings or
animals. There are generally three types
of regulated medical waste: (1)
Infectious waste; (2) pathological waste;
and (3) trace chemotherapy waste.
Infectious waste is waste that has come
into contact with bodily fluids and
‘‘sharps’’ waste, such as syringes and
scalpels. Pathological waste is
anatomical parts, and trace
chemotherapy waste is small amounts of
chemical compounds used to treat
cancer patients and the equipment used
to administer the compounds. Infectious
waste comprises approximately 90
percent of the regulated medical waste
generated in the United States.
9. State and Federal governments
heavily regulate the collection and
treatment of regulated medical waste.
They prescribe how each type of
regulated medical waste must be stored,
collected, and treated. Providers of
infectious waste collection and
treatment services are required to be
licensed by various state and Federal
regulatory agencies before they can offer
such services.
10. Regulated medical waste must be
stored separately from other types of
waste, and each type of regulated
medical waste must be stored separately
from the other types in specially marked
and sealed containers. Collection and
transport of regulated medical waste to
treatment facilities must be performed
by state-approved companies.
11. State-approved treatment facilities
must be used to render regulated
medical waste non-infectious. Failure to
use state-approved treatment facilities
subjects both the generator of the
infectious waste and the infectious
waste collection and treatment service
provider to criminal prosecution, fines,
damage actions, and potentially high
clean-up costs.
12. Autoclaves are the most prevalent
treatment technology for infectious
waste. An autoclave uses steam
sterilization combined with pressure to
render infectious waste non-infectious.
Because autoclaving is a reliable and
long-proven technology, it has become
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the preferred choice for treating
infectious waste.
13. The infectious waste collection
and treatment services industry
categorizes customers according to the
amount of infectious waste they
generate. LQG customers typically are
hospitals, large laboratories, and other
large medical facilities that generate
large amounts of infectious waste. LQG
customers often need collection to occur
on a daily basis, or at least several times
a week, and must receive continuous
supplies of containers with sizeable
storage capacity from their service
providers.
14. LQG customers require their
service providers to perform both
infectious waste collection and
treatment. They also require their
providers to meet strict standards to
ensure they have sufficient technical
capability, knowledge, and financial
resources. For example, an LQG
customer typically requires an
infectious waste collection and
treatment service provider to have: (a)
An adequate infrastructure to serve the
customer’s needs, including trucks,
storage containers, transfer stations,
electronic equipment capable of
monitoring and tracking each type of
waste, and personnel with a variety of
expertise to support the infrastructure;
(b) an established reputation for
providing reliable and timely collection
and treatment for LQG customers; (c) its
own infectious waste treatment facility
to minimize the number of companies
that handle the waste, thereby reducing
the possibility that the waste is
mishandled; and (d) substantial liability
insurance that meets all Federal and
state regulatory requirements governing
infectious waste.
15. Collection and treatment
providers bid for each LQG customer’s
business separately, and an infectious
waste collection and treatment service
provider can identify the specific
competitive conditions that apply to
each LQG customer, including which
potential competitors can serve that
LQG customer. Infectious waste
collection and treatment service
providers for LQG customers can and do
price discriminate based on an LQG
customer’s requirements and the
number of other competitors available to
provide such services.
16. A small but significant increase in
the price of infectious waste collection
and treatment services for LQG
customers would not cause LQG
customers to move sufficient volumes of
infectious waste to another type of
collection and treatment service so as to
make such a price increase unprofitable.
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17. Accordingly, the provision of
infectious waste collection and
treatment services for LQG customers is
a line of commerce and a relevant price
discrimination service market within
the meaning of Section 7 of the Clayton
Act.
B. The Relevant Geographic Market
18. The geographic market for the
provision of infectious waste collection
and treatment services for LQG
customers is largely defined by
transportation costs. Infectious waste
collection and treatment companies rely
on trucks to transport waste from
customer sites to their treatment
facilities. Transfer stations enable
service providers to transfer their waste
into tractor-trailers and more costeffectively to transport their waste to
treatment facilities. Typically, the
greater the distance between an LQG
customer’s operations and the service
provider’s treatment or transfer facility,
the less price competitive the provider
is.
19. For LQG customers served by
MedServe in Kansas, Missouri,
Nebraska, and Oklahoma, the only
competitive alternative is Stericycle. In
these states, no other infectious waste
collection and treatment service
provider has a facility located within
approximately 300 miles of Stericycle’s
or MedServe’s facilities.
20. In the states of Kansas, Missouri,
Nebraska, and Oklahoma, LQG
customers would not switch to a more
distant infectious waste collection and
treatment service provider in sufficient
numbers so as to make a small but
significant increase in price
unprofitable.
21. Accordingly, the states of Kansas,
Missouri, Nebraska, and Oklahoma are a
relevant geographic market within the
meaning of Section 7 of the Clayton Act.
C. Anticompetitive Effects of the
Acquisition
22. In the states of Kansas, Missouri,
Nebraska, and Oklahoma, the market for
the provision of infectious waste
collection and treatment services for
LQG customers is highly concentrated.
Following the acquisition, Stericycle
would become the monopoly provider
of infectious waste collection and
treatment services for LQG customers in
these states.
23. Vigorous price competition
between Stericycle and MedServe in the
provision of infectious waste collection
and treatment services has benefited
LQG customers in Kansas, Missouri,
Nebraska, and Oklahoma. Stericycle and
MedServe are each other’s only rivals,
directly competing on price and quality
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of service in the provision of infectious
waste collection and treatment services
for LQG customers.
24. Therefore, the proposed
acquisition will eliminate the
competition between Stericycle and
MedServe; reduce the number of
providers of infectious waste collection
and treatment services for LQG
customers from two to one; and enable
Stericycle to establish a monopoly in
the provision of such services, leading
to higher prices and lower quality of
service for LQG customers in Kansas,
Missouri, Nebraska, and Oklahoma, in
violation of Section 7 of the Clayton
Act.
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D. Entry Into Collection and Treatment
of Infectious Waste Generated by LQG
Customers
25. Successful entry into the
provision of collection and treatment
services for infectious waste for LQG
customers in Kansas, Missouri,
Nebraska, and Oklahoma would be
difficult, time-consuming, and costly. A
prospective provider of infectious waste
collection and treatment services for
LQG customers faces substantial
financial and permitting requirements to
build a facility and the infrastructure
needed to serve LQG customers. It also
must have an established reputation for
handling the large amounts of infectious
waste produced by LQG customers.
26. A provider of infectious waste
collection and treatment services for
LQG customers in Kansas, Missouri,
Nebraska, and Oklahoma must establish
a treatment facility that contains a
treatment technology, such as an
autoclave, with sufficient capacity for
treating large volumes of infectious
waste. In addition to the capital costs of
the treatment unit, local zoning and
state permits are required.
27. A provider of infectious waste
collection and treatment services for
LQG customers also must have an
infrastructure of trucks, transfer
stations, and electronic equipment
capable of collecting, transporting,
treating and disposing, and monitoring
and tracking the infectious waste.
28. A provider of infectious waste
collection and treatment services for
LQG customers must develop a
reputation and record of reliably
collecting and treating large volumes of
infectious waste in compliance with
state and Federal regulations.
29. A provider of infectious waste
collection and treatment services for
LQG customers must have the financial
capability to indemnify LQG customers
for any environmental fines or accidents
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resulting from the collection,
transportation, and treatment of the
infectious waste.
30. Obtaining the necessary permits
and building an autoclave facility,
establishing the infrastructure to serve
LQG customers, and developing a
reputation and record of service and
compliance would require in excess of
two years.
31. Entry into the provision of
infectious waste collection and
treatment services for LQG customers in
Kansas, Missouri, Nebraska, and
Oklahoma would not be timely, likely,
or sufficient to counter anticompetitive
price increases or diminished quality of
service that Stericycle could impose
after the proposed acquisition.
V. Violation Alleged
32. The United States incorporates the
allegations of paragraphs 1 through 31
above.
33. Stericycle’s proposed acquisition
of all of MedServe’s voting securities
and infectious waste collection and
treatment assets in the states of Kansas,
Missouri, Nebraska, and Oklahoma will
substantially lessen competition and
tend to create a monopoly in interstate
trade and commerce in violation of
Section 7 of the Clayton Act, 15 U.S.C.
18.
34. Unless restrained, the transaction
will have the following anticompetitive
effects, among others:
a. Actual and potential competition
between Stericycle and MedServe in the
provision of infectious waste collection
and treatment services for LQG
customers in the states of Kansas,
Missouri, Nebraska, and Oklahoma will
be eliminated;
b. Competition generally in the
provision of infectious waste collection
and treatment services for LQG
customers in the states of Kansas,
Missouri, Nebraska, and Oklahoma will
be substantially lessened; and
c. Prices for infectious waste
collection and treatment services for
LQG customers in the states of Kansas,
Missouri, Nebraska, and Oklahoma will
likely increase, and service likely will
be reduced.
VI. Requested Relief
35. Plaintiffs request:
a. That Stericycle’s proposed
acquisition of MedServe be adjudged
and decreed to be unlawful and in
violation of Section 7 of the Clayton
Act, 15 U.S.C. 18;
b. That defendants and all persons
acting on their behalf be permanently
enjoined and restrained from
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consummating the proposed acquisition
of MedServe by Stericycle, or from
entering into or carrying out any
contract, agreement, plan, or
understanding, the effect of which
would be to merge the voting securities
or assets of the defendants;
c. That plaintiffs receive such other
and further relief as the case requires
and the Court deems just and proper;
and
d. That plaintiffs recover the costs of
this action.
Dated: November 30, 2009.
Respectfully submitted,
For Plaintiff United States of America.
/s/ lllllllllllllllllll
Christine A. Varney,
Assistant Attorney General, D.C. Bar #
435204.
/s/ lllllllllllllllllll
Maribeth Petrizzi,
Chief, Litigation II Section.
/s/ lllllllllllllllllll
Molly S. Boast,
Deputy Assistant Attorney General.
/s/ lllllllllllllllllll
Dorothy B. Fountain,
Assistant Chief, Litigation II Section, D.C. Bar
# 439469.
/s/ lllllllllllllllllll
J. Robert Kramer II,
Director of Operations.
/s/ lllllllllllllllllll
Frederick H. Parmenter
Stephen A. Harris
Carolyn Davis
Leslie D. Peritz
Jay D. Owen,
Attorneys. U.S. Department of Justice,
Antitrust Division, Litigation II Section,
Suite 8700, 450 Fifth Street, NW.,
Washington, DC 20530. Tel: (202) 307–
0924, Fax: (202) 307–6583, E-mail:
Frederick.Parmenter@usdoj.gov.
For Plaintiff State of Missouri.
Chris Koster,
Attorney General.
By:
/s/ lllllllllllllllllll
Anne E. Schneider,
Assistant Attorney General, State of Missouri,
P.O. Box 899, Jefferson City, MO 65102,
Tel: (573) 751–8455, Fax: (573) 751–2041,
E-mail: Anne.Schneider@ago.mo.gov.
For Plaintiff State of Nebraska.
Jon Bruning,
Attorney General.
By:
/s/ lllllllllllllllllll
Leslie C. Levy,
Assistant Attorney General, 2115 State
Capitol Building, Lincoln, NE 68509–8920,
Tel.: (402) 471–2811, Fax: (402) 471–4725,
E-mail: Leslie.Levy@nebraska.gov.
IN THE UNITED STATES DISTRICT
COURT FOR THE DISTRICT OF
COLUMBIA
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UNITED STATES OF AMERICA, STATE OF MISSOURI, and STATE OF NEBRASKA, Plaintiffs, v. STERICYCLE,
INC., ATMW ACQUISITION CORP., MEDSERVE, INC., and AVISTA CAPITAL PARTNERS, L.P., Defendants.
Proposed Final Judgement
Whereas, plaintiffs, the United States
of America, the State of Missouri, and
the State of Nebraska, filed their
Complaint on November 30, 2009;
plaintiffs and defendants, Stericycle,
Inc. and ATMW Acquisition Corp., and
MedServe, Inc. and Avista Capital
Partners, L.P., by their respective
attorneys, have consented to the entry of
this Final Judgment without trial or
adjudication of any issue of fact or law;
and without this Final Judgment
constituting any evidence against or
admission by any party regarding any
issue of law or fact;
And Whereas, defendants agree to be
bound by the provisions of this Final
Judgment pending its approval by the
Court;
And Whereas, the essence of this
Final Judgment is the prompt and
certain divestiture of the Divestiture
Assets to assure that competition is not
substantially lessened;
And Whereas, the United States
requires defendants to make certain
divestitures for the purpose of
remedying the loss of competition
alleged in the Complaint;
And Whereas, defendants have
represented to the United States that the
divestitures required below can and will
be made, and that defendants will later
raise no claim of hardship or difficulty
as grounds for asking the Court to
modify any of the divestiture provisions
contained below;
Now, Therefore, before any testimony
is taken, without trial or adjudication of
any issue of fact or law, and upon
consent of the parties, it is hereby
Ordered, Adjudged, and Decreed:
I. Jurisdiction
This Court has jurisdiction over the
subject matter of and each of the parties
to this action. The Complaint states a
claim upon which relief may be granted
against the defendants under Section 7
of the Clayton Act, 15 U.S.C. 18, as
amended.
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II. Definitions
As used in this Final Judgment:
A. ‘‘Acquirer’’ means the entity to
which defendants shall divest the
Divestiture Assets.
B. ‘‘Stericycle’’ means defendant
Stericycle, Inc., a Delaware corporation
with its principal place of business in
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Lake Forest, Illinois, and ATMW
Acquisition Corp. (a corporation formed
to facilitate the acquisition), and their
successors, assigns, subsidiaries,
divisions, groups, affiliates,
partnerships, and joint ventures, and all
of their directors, officers, managers,
agents, and employees.
C. ‘‘MedServe’’ means defendant
MedServe, Inc., a Delaware corporation
with its principal place of business in
Bellaire, Texas, and Avista Capital
Partners, L.P. formed to facilitate the
acquisition, and their successors,
assigns, subsidiaries, divisions, groups,
affiliates, partnerships, and joint
ventures, and all of their directors,
officers, managers, agents, and
employees.
D. ‘‘Infectious Waste’’ means regulated
medical waste that is generated in the
diagnosis, treatment, or immunization
of human beings or animals and that has
come into contact with bodily fluids,
and ‘‘sharps’’ waste, such as syringes and
scalpels.
E. ‘‘Treatment’’ means the sterilization
of infectious waste at a state-approved
treatment facility, including the use of
transfer stations to facilitate the
shipment of infectious waste to other
treatment sites.
F. ‘‘Large Quantity Generator
Customer’’ or ‘‘LQG Customer’’ means
any customer that spends $1000 or more
per month on infectious waste
collection and treatment services.
G. ‘‘Divestiture Assets’’ means:
1. The following facilities:
a. MedServe’s Newton, Kansas
autoclave facility, located at 1021 South
Spencer Avenue, Newton, Kansas
67114;
b. MedServe’s Kansas City, Kansas
transfer station, located at 200 Funston
Road, Suite B, Kansas City, Kansas
66115;
c. MedServe’s Oklahoma City,
Oklahoma transfer station, located at
8800 SW 8th Street, Oklahoma City,
Oklahoma 73128;
d. MedServe’s Omaha, Nebraska
transfer station, located at 13824–C
Plaza, Omaha, Nebraska 68144; and
e. MedServe’s Booneville, Missouri
transfer station, located at 680 Al
Bersted Drive, Booneville, Missouri
65233;
2. All tangible assets at the MedServe
facilities listed in Paragraph II(G)(1),
including all research and development
activities, equipment, and fixed assets,
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CASE NO.: 1:09-cv-02268,
JUDGE: John D. Bates,
DECK TYPE: Antitrust,
DATE STAMP: November 30, 2009.
real property (leased or owned),
equipment, personal property, inventory
(containers), office furniture, materials,
supplies, on- or off-site warehouses or
storage facilities; all licenses, permits,
and authorizations issued by any
governmental organization relating to
the facilities; all lists of MedServe LQG
customers; all MedServe LQG customer
contracts, accounts, and credit records;
all other records; and all trucks and
other vehicles assigned to the facilities
as of May 9, 2009; and
3. All intangible assets associated
with the MedServe facilities listed in
Paragraph II(G)(1), including, but not
limited to, all contractual rights,
patents, licenses and sublicenses,
intellectual property, technical
information, computer software
(including waste monitoring software
and management information systems)
and related documentation, know-how,
trade secrets, drawings, blueprints,
designs, design protocols, specifications
for materials, specifications for parts
and devices, safety procedures for the
handling of materials and substances,
quality assurance and control
procedures, design tools and simulation
capability, all manuals and technical
information provided to employees,
customers, suppliers, agents or
licensees.
III. Applicability
A. This Final Judgment applies to
Stericycle and MedServe, as defined
above, and all other persons in active
concert or participation with either of
them, who receive actual notice of this
Final Judgment by personal service or
otherwise.
B. If, prior to complying with Sections
IV and V of this Final Judgment,
defendants sell or otherwise dispose of
all or substantially all of their assets or
of lesser business units that include the
Divestiture Assets, they shall require the
purchaser to be bound by the provisions
of this Final Judgment. Defendants need
not obtain such an agreement from the
Acquirer of the assets divested pursuant
to this Final Judgment.
IV. Divestitures
A. Defendants are ordered and
directed, within ninety (90) calendar
days after the filing of the Complaint in
this matter, or five (5) calendar days
after notice of the entry of this Final
Judgment by the Court, whichever is
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later, to divest the Divestiture Assets in
a manner consistent with this Final
Judgment to an Acquirer acceptable to
the United States in its sole discretion,
after consultation with the State of
Missouri and the State of Nebraska. The
United States, in its sole discretion, after
consultation with the State of Missouri
and the State of Nebraska, may agree to
one or more extensions of this time
period not to exceed sixty (60) calendar
days in total, and shall notify the Court
in such circumstances. Defendants agree
to use their best efforts to divest the
Divestiture Assets as expeditiously as
possible.
B. In accomplishing the divestitures
ordered by this Final Judgment,
defendants promptly shall make known,
by usual and customary means, the
availability of the Divestiture Assets.
Defendants shall inform any person
making an inquiry regarding a possible
purchase of the Divestiture Assets that
they are being divested pursuant to this
Final Judgment and provide that person
with a copy of this Final Judgment.
Defendants shall offer to furnish to all
prospective Acquirers, subject to
customary confidentiality assurances,
all information and documents relating
to the Divestiture Assets customarily
provided in a due diligence process
except such information or documents
subject to the attorney-client privilege or
work-product doctrine. Defendants shall
make available such information to the
United States at the same time that such
information is made available to any
other person.
C. Defendants shall provide the
Acquirer and the United States
information relating to the personnel
involved in the operation and
management of the Divestiture Assets to
enable the Acquirer to make offers of
employment. Defendants shall not
interfere with any negotiations by the
Acquirer to employ or contract with any
defendant employee whose primary
responsibility is the operation or
management of the Divestiture Assets.
D. Defendants shall permit
prospective Acquirers of the Divestiture
Assets to have reasonable access to
personnel and to make inspections of
the physical facilities of the Divestiture
Assets; access to any and all
environmental, zoning, and other permit
documents and information; and access
to any and all financial, operational or
other documents and information
customarily provided as part of a due
diligence process.
E. Defendants shall warrant to the
Acquirer that each asset will be
operational on the date of sale.
F. Defendants shall not take any
action that will impede in any way the
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permitting, operation or divestiture of
the Divestiture Assets.
G. Defendants shall warrant to the
Acquirer that there are no material
defects in the environmental, zoning or
other permits pertaining to the
operation of the Divestiture Assets, and
that following the sale of the Divestiture
Assets, defendants will not undertake,
directly or indirectly, any challenges to
the environmental, zoning, or other
permits relating to the operation of the
Divestiture Assets.
H. Unless the United States, after
consultation with the State of Missouri
and the State of Nebraska, otherwise
consents in writing, the divestitures
pursuant to Section IV, or by trustee
appointed pursuant to Section V, of this
Final Judgment, shall be made to a
single Acquirer and shall include all the
Divestiture Assets, and shall be
accomplished in such a way as to satisfy
the United States, in its sole discretion,
after consultation with the State of
Missouri and the State of Nebraska, that
the divestitures will achieve the
purposes of this Final Judgment and
that the Divestiture Assets can and will
be used by the Acquirer as part of a
viable, ongoing business providing
infectious waste collection and
treatment services for LQG customers
located in Kansas, Missouri, Nebraska,
and Oklahoma. The divestitures,
whether pursuant to Section IV or
Section V of this Final Judgment:
1. Shall be made to the Acquirer that,
in the United States’s sole judgment,
after consultation with the State of
Missouri and the State of Nebraska, has
the intent and capability (including the
necessary managerial, operational,
technical and financial capability) of
competing effectively in the business of
providing infectious waste collection
and treatment services for LQG
customers; and
2. Shall be accomplished so as to
satisfy the United States, in its sole
discretion, after consultation with the
State of Missouri and the State of
Nebraska, that none of the terms of any
agreement between the Acquirer and
defendants gives defendants the ability
unreasonably to raise the Acquirer’s
costs, to lower the Acquirer’s efficiency,
or otherwise to interfere in the ability of
the Acquirer to compete effectively.
V. Appointment of Trustee
A. If defendants have not divested the
Divestiture Assets within the time
period specified in Section IV,
defendants shall notify the United
States of that fact in writing. Upon
application of the United States, the
Court shall appoint a trustee selected by
the United States and approved by the
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5125
Court to effect the sale of the Divestiture
Assets.
B. After the appointment of a trustee
becomes effective, only the trustee shall
have the right to sell the Divestiture
Assets. The trustee shall have the power
and authority to accomplish the
divestitures to an Acquirer acceptable to
the United States, after consultation
with the State of Missouri and the State
of Nebraska, at such price and on such
terms as are then obtainable upon
reasonable effort by the trustee, subject
to the provisions of Sections IV, V and
VI of this Final Judgment, and shall
have such other powers as this Court
deems appropriate. Subject to Section V,
Paragraph D, of this Final Judgment, the
trustee may hire at the defendants’ cost
and expense any investment bankers,
attorneys, or other agents, who shall be
solely accountable to the trustee,
reasonably necessary in the trustee’s
judgment to assist in the divestitures.
C. Defendants shall not object to a sale
by the trustee on any ground other than
the trustee’s malfeasance. Any such
objections by defendants must be
conveyed in writing to the United States
and the trustee within ten (10) calendar
days after the trustee has provided the
notice required under Section VI.
D. The trustee shall serve at the cost
and expense of defendants, on such
terms and conditions as the United
States approves, and shall account for
all monies derived from the sale of the
assets sold by the trustee and all costs
and expenses so incurred. After
approval by the Court of the trustee’s
accounting, including fees for its
services and those of any professionals
and agents retained by the trustee, all
remaining money shall be paid to
defendants and the trust shall then be
terminated. The compensation of the
trustee and any professionals and agents
retained by the trustee shall be
reasonable in light of the value of the
Divestiture Assets and based on a fee
arrangement providing the trustee with
an incentive based on the price and
terms of the divestitures and the speed
with which it is accomplished, but
timeliness is paramount.
E. Defendants shall use their best
efforts to assist the trustee in
accomplishing the required divestitures.
The trustee and any consultants,
accountants, attorneys, and other
persons retained by the trustee shall
have full and complete access to the
personnel, books, records, and facilities
of the business to be divested, and
defendants shall develop financial and
other information relevant to such
business as the trustee may reasonably
request, subject to reasonable protection
for trade secret or other confidential
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research, development, or commercial
information. Defendants shall take no
action to interfere with or to impede the
trustee’s accomplishment of the
divestitures.
F. After its appointment, the trustee
shall file monthly reports with the
United States, the State of Missouri, the
State of Nebraska, and the Court setting
forth the trustee’s efforts to accomplish
the divestitures ordered under this Final
Judgment. To the extent such reports
contain information that the trustee
deems confidential, such reports shall
not be filed in the public docket of the
Court. Such reports shall include the
name, address, and telephone number of
each person who, during the preceding
month, made an offer to acquire,
expressed an interest in acquiring,
entered into negotiations to acquire, or
was contacted or made an inquiry about
acquiring, any interest in the Divestiture
Assets, and shall describe in detail each
contact with any such person. The
trustee shall maintain full records of all
efforts made to divest the Divestiture
Assets.
G. If the trustee has not accomplished
the divestitures ordered under this Final
Judgment within six (6) months after its
appointment, the trustee shall promptly
file with the Court a report setting forth:
(1) The trustee’s efforts to accomplish
the required divestitures; (2) the
reasons, in the trustee’s judgment, why
the required divestitures have not been
accomplished; and (3) the trustee’s
recommendations. To the extent such
reports contain information that the
trustee deems confidential, such reports
shall not be filed in the public docket
of the Court. The trustee shall at the
same time furnish such report to the
United States, which shall have the
right to make additional
recommendations consistent with the
purpose of the trust. The Court
thereafter shall enter such orders as it
shall deem appropriate to carry out the
purpose of the Final Judgment, which
may, if necessary, include extending the
trust and the term of the trustee’s
appointment by a period requested by
the United States.
VI. Notice of Proposed Divestitures
A. Within two (2) business days
following execution of a definitive
divestiture agreement, defendants or the
trustee, whichever is then responsible
for effecting the divestitures required
herein, shall notify the United States,
the State of Missouri, and the State of
Nebraska of any proposed divestiture
required by Section IV or V of this Final
Judgment. If the trustee is responsible,
it shall similarly notify defendants. The
notice shall set forth the details of the
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proposed divestitures and list the name,
address, and telephone number of each
person not previously identified who
offered or expressed an interest in or
desire to acquire any ownership interest
in the Divestiture Assets, together with
full details of the same.
B. Within fifteen (15) calendar days of
receipt of such notice by the United
States, the State of Missouri, and the
State of Nebraska, the United States may
request from defendants, the proposed
Acquirer, any other third party, or the
trustee, if applicable, additional
information concerning the proposed
divestitures, the proposed Acquirer and
any other potential Acquirer.
Defendants and the trustee shall furnish
any additional information requested
within fifteen (15) calendar days of the
receipt of the request, unless the parties
shall otherwise agree.
C. Within thirty (30) calendar days
after receipt of the notice or within
twenty (20) calendar days after the
United States has been provided the
additional information requested from
defendants, the proposed Acquirer, any
third party, and the trustee, whichever
is later, the United States shall provide
written notice to defendants and the
trustee, if there is one, stating whether
or not it objects to the proposed
divestitures. If the United States, after
consultation with the State of Missouri
and the State of Nebraska, provides
written notice that it does not object, the
divestitures may be consummated,
subject only to defendants’ limited right
to object to the sale under paragraph
V(C) of this Final Judgment. Absent
written notice that the United States
does not object to the proposed Acquirer
or upon objection by the United States,
a divestiture proposed under Section IV
or Section V shall not be consummated.
Upon objection by defendants under
paragraph V(C), a divestiture proposed
under Section V shall not be
consummated unless approved by the
Court.
VII. Notice of Future Acquisitions
A. Unless such transaction is
otherwise subject to the reporting and
waiting period requirements of the HartScott-Rodino Antitrust Improvements
Act of 1976, as amended, 15 U.S.C. 18a
(the ‘‘HSR Act’’), Stericycle, without
providing advance notification to the
United States, the State of Missouri, and
the State of Nebraska, shall not directly
or indirectly acquire, any (1) interest in
any business located in Kansas,
Missouri, Nebraska, and Oklahoma that
is engaged in the collection and
treatment of infectious waste; (2) other
than in the ordinary course of business,
assets located in Kansas, Missouri,
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Fmt 4703
Sfmt 4703
Nebraska, and Oklahoma that are used
in the collection and treatment of
infectious waste; or (3) capital stock or
voting securities of any person that, at
any time during the twelve (12) months
immediately preceding such
acquisition, was engaged in the
collection and treatment of infectious
waste in Kansas, Missouri, Nebraska, or
Oklahoma, where that person’s annual
revenues in these states from the
collection and treatment of infectious
waste were in excess of $500,000.
B. Such notification shall be provided
to the United States, the State of
Missouri, and the State of Nebraska in
the same format as, and per the
instructions relating to the Notification
and Report Form set forth in the
Appendix to Part 803 of Title 16 of the
Code of Federal Regulations as
amended, except that the information
requested in Items 5 through 9 of the
instructions must be provided only
about the collection and treatment of
infectious waste. Notification shall be
provided at least thirty (30) calendar
days prior to acquiring any such
interest, and shall include, beyond what
may be required by the applicable
instructions, the names of the principal
representatives of the parties to the
agreement who negotiated the
agreement, and any management or
strategic plans discussing the proposed
transaction. If within the 30-day period
after notification, representatives of the
United States make a written request for
additional information, Stericycle shall
not consummate the proposed
transaction or agreement until thirty
(30) calendar days after submitting all
such additional information. Early
termination of the waiting periods in
this paragraph may be requested and,
where appropriate, granted in the same
manner as is applicable under the
requirements and provisions of the HSR
Act and rules promulgated thereunder.
This Section shall be broadly construed
and any ambiguity or uncertainty
regarding the filing of notice under this
Section shall be resolved in favor of
filing notice.
VIII. Financing
Defendants shall not finance all or
any part of any purchase made pursuant
to Section IV or V of this Final
Judgment.
IX. Hold Separate
Until the divestitures required by this
Final Judgment have been
accomplished, defendants shall take all
steps necessary to comply with the Hold
Separate Stipulation and Order entered
by this Court. Defendants shall take no
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XI. Compliance Inspection
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action that would jeopardize the
divestitures ordered by this Court.
X. Affidavits
A. Within twenty (20) calendar days
of the filing of the Complaint in this
matter, and every thirty (30) calendar
days thereafter until the divestitures
have been completed under Section IV
or V, defendants shall deliver to the
United States, the State of Missouri, and
the State of Nebraska an affidavit as to
the fact and manner of its compliance
with Section IV or V of this Final
Judgment. Each such affidavit shall
include the name, address, and
telephone number of each person who,
during the preceding thirty (30)
calendar days, made an offer to acquire,
expressed an interest in acquiring,
entered into negotiations to acquire, or
was contacted or made an inquiry about
acquiring, any interest in the Divestiture
Assets, and shall describe in detail each
contact with any such person during
that period. Each such affidavit shall
also include a description of the efforts
defendants have taken to solicit buyers
for the Divestiture Assets, and to
provide required information to
prospective Acquirers, including the
limitations, if any, on such information.
Assuming the information set forth in
the affidavit is true and complete, any
objection by the United States, after
consultation with the State of Missouri
and the State of Nebraska, to
information provided by defendants,
including limitation on information,
shall be made within fourteen (14)
calendar days of receipt of such
affidavit.
B. Within twenty (20) calendar days
of the filing of the Complaint in this
matter, defendants shall deliver to the
United States an affidavit that describes
in reasonable detail all actions
defendants have taken and all steps
defendants have implemented on an
ongoing basis to comply with Section IX
of this Final Judgment. Defendants shall
deliver to the United States, the State of
Missouri, and the State of Nebraska, an
affidavit describing any changes to the
efforts and actions outlined in
defendants’ earlier affidavits filed
pursuant to this section within fifteen
(15) calendar days after the change is
implemented.
C. Defendants shall keep all records of
all efforts made to preserve and divest
the Divestiture Assets until one year
after such divestitures have been
completed.
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A. For the purposes of determining or
securing compliance with this Final
Judgment, or of determining whether
the Final Judgment should be modified
or vacated, and subject to any legally
recognized privilege, from time to time
authorized representatives of the United
States Department of Justice Antitrust
Division (‘‘DOJ’’), including consultants
and other persons retained by the
United States, shall, upon written
request of an authorized representative
of the Assistant Attorney General in
charge of the Antitrust Division, and on
reasonable notice to defendants, be
permitted:
1. access during defendants’ office
hours to inspect and copy, or at the
option of the United States, to require
defendants to provide hard copy or
electronic copies of, all books, ledgers,
accounts, records, data, and documents
in the possession, custody, or control of
defendants, relating to any matters
contained in this Final Judgment; and
2. to interview, either informally or on
the record, defendants’ officers,
employees, or agents, who may have
their individual counsel present,
regarding such matters. The interviews
shall be subject to the reasonable
convenience of the interviewee and
without restraint or interference by
defendants.
B. Upon the written request of an
authorized representative of the
Assistant Attorney General in charge of
the Antitrust Division, defendants shall
submit written reports or responses to
written interrogatories, under oath if
requested, relating to any of the matters
contained in this Final Judgment as may
be requested.
C. No information or documents
obtained by the means provided in this
section shall be divulged by the United
States to any person other than an
authorized representative of the
executive branch of the United States,
except in the course of legal proceedings
to which the United States is a party
(including grand jury proceedings), or
for the purpose of securing compliance
with this Final Judgment, or as
otherwise required by law.
D. If at the time information or
documents are furnished by defendants
to the United States, defendants
represent and identify in writing the
material in any such information or
documents to which a claim of
protection may be asserted under Rule
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5127
26(c)(1)(G) of the Federal Rules of Civil
Procedure, and defendants mark each
pertinent page of such material, ‘‘Subject
to claim of protection under Rule
26(c)(1)(G) of the Federal Rules of Civil
Procedure,’’ then the United States shall
give defendants ten (10) calendar days
notice prior to divulging such material
in any legal proceeding (other than a
grand jury proceeding).
XII. No Reacquisition
During the term of this Final
Judgment, defendants may not reacquire
any part of the Divestiture Assets, nor
may any defendant participate in any
other transaction that would result in a
combination, merger, or other joining
together of any part of the Divestiture
Assets with assets of the divesting
company.
XIII. Retention of Jurisdiction
This Court retains jurisdiction to
enable any party to this Final Judgment
to apply to this Court at any time for
further orders and directions as may be
necessary or appropriate to carry out or
construe this Final Judgment, to modify
any of its provisions, to enforce
compliance, and to punish violations of
its provisions.
XIV. Expiration of Final Judgment
Unless this Court grants an extension,
this Final Judgment shall expire ten (10)
years from the date of its entry.
XV. Public Interest Determination
Entry of this Final Judgment is in the
public interest. The parties have
complied with the requirements of the
Antitrust Procedures and Penalties Act,
15 U.S.C. 16, including making copies
available to the public of this Final
Judgment, the Competitive Impact
Statement, and any comments thereon
and the United States’s responses to
comments. Based upon the record
before the Court, which includes the
Competitive Impact Statement and any
comments and response to comments
filed with the Court, entry of this Final
Judgment is in the public interest.
Date: llllllllllllllll
Court approval subject to procedures of
Antitrust Procedures and Penalties Act,
15 U.S.C. 16
llllllllllllllllll
l
United States District Judge
United States District Court for the
District of Columbia
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UNITED STATES OF AMERICA, STATE OF MISSOURI, and STATE OF NEBRASKA, Plaintiffs, v. STERICYCLE, INC., ATMW ACQUISITION CORP., MEDSERVE, INC., and AVISTA
CAPITAL PARTNERS L.P., Defendants.
Competitive Impact Statement
Plaintiff United States of America
(‘‘United States’’), pursuant to Section
2(b) of the Antitrust Procedures and
Penalties Act (‘‘APPA’’ or ‘‘Tunney Act’’),
15 U.S.C. 16(b)-(h), files this
Competitive Impact Statement relating
to the proposed Final Judgment
submitted for entry in this civil antitrust
proceeding.
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I. Nature and Purpose of the Proceeding
Defendant Stericycle, Inc., through
ATMW Acquisition Corp., and
defendant MedServe, Inc., through
Avista Capital Partners, L.P., entered
into a stock purchase agreement dated
May 9, 2009, pursuant to which
Stericycle would acquire all of the
voting shares of MedServe, valued at
$185 million. The United States, and the
State of Missouri and the State of
Nebraska (‘‘States’’), filed a civil antitrust
Complaint on November 30, 2009,
seeking to enjoin the proposed
acquisition. The Complaint alleged that
the likely effect of the acquisition would
be to substantially lessen competition in
the provision of infectious waste
collection and treatment services for
large quantity generator (‘‘LQG’’)
customers in the states of Kansas,
Missouri, Nebraska, and Oklahoma, in
violation of Section 7 of the Clayton
Act, 15 U.S.C. 18. This loss of
competition would result in higher
prices and reduced service for these
customers of infectious waste collection
and treatment services.
With the filing of the Complaint in
this case, the United States and the
States also filed a Hold Separate
Stipulation and Order and proposed
Final Judgment, which are designed to
eliminate the anticompetitive effects of
the acquisition. Under the proposed
Final Judgment, explained more fully
below, Stericycle and MedServe are
required within ninety (90) days after
the filing of the Complaint, or five (5)
days after notice of the entry of the Final
Judgment by the Court, whichever is
later, to divest, as a viable business, all
of the MedServe infectious waste
collection and treatment assets in
Kansas, Missouri, Nebraska, and
Oklahoma. Under the terms of the Hold
Separate Stipulation and Order,
Stericycle and MedServe are required to
take certain steps to ensure that the
assets to be divested will be preserved
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and held separate from their other assets
and businesses.
The United States, the States, and the
defendants have stipulated that the
proposed Final Judgment may be
entered after compliance with the
APPA. Entry of the proposed Final
Judgment would terminate this action,
except that the Court would retain
jurisdiction to construe, modify, or
enforce the provisions of the proposed
Final Judgment and to punish violations
thereof.
II. Description of the Events Giving Rise
to the Alleged Violation
A. The Defendants and the Proposed
Transaction
Stericycle is a Delaware corporation
with its principal place of business in
Lake Forest, Illinois. Stericycle, a multinational company, is the largest
provider of infectious waste collection
and treatment services in the United
States, with operations in nearly all of
the contiguous 48 states, including 46
treatment facilities and 80 transfer and
collection sites. In 2008, Stericycle
reported total worldwide sales of
approximately $1.1 billion, of which
approximately 78 percent were
generated in the United States. ATMW
Acquisition Corp. is a corporation
formed by Stericycle to facilitate its
acquisition of MedServe.
MedServe is a Delaware corporation
with its principal place of business in
Bellaire, Texas. MedServe is the secondlargest provider of infectious waste
collection and treatment services in the
United States, with operations in 25
states that include eight treatment
facilities and 18 transfer and collection
sites. In 2008, MedServe had total
revenues of about $35 million. Avista
Capital Partners, L.P. is an entity formed
by MedServe to facilitate the acquisition
of MedServe by Stericycle.
The proposed transaction, as agreed to
by defendants on May 9, 2009, would
substantially lessen competition in the
provision of infectious waste collection
and treatment services for LQG
customers in the states of Missouri,
Nebraska, Oklahoma, and Kansas. This
acquisition is the subject of the
Complaint and proposed Final
Judgment filed by the United States and
the States on November 30, 2009.
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CASE NO.: 1:09-cv-02268,
JUDGE: Hon. John D.
Bates, DECK TYPE: Antitrust, DATE STAMP.
B. The Competitive Effects of the
Transaction
1. Relevant Service Market: Infectious
Waste Collection and Treatment
Services for LQG Customers
Regulated medical waste is waste
generated in the diagnosis, treatment, or
immunization of human beings or
animals. There are three types of
regulated medical waste: (1) Infectious
waste; (2) pathological waste; and (3)
trace chemotherapy waste. Infectious
waste is waste that comes into contact
with bodily fluids and ‘‘sharps’’ waste,
such as syringes and scalpels.
Pathological waste is anatomical parts,
and trace chemotherapy waste is small
amounts of chemical compounds used
to treat cancer patients and the
equipment used to administer the
compounds. Infectious waste comprises
approximately 90 percent of all
regulated medical waste generated in
the United States.
State and Federal governments
heavily regulate the collection and
treatment of regulated medical waste.
They prescribe how each type of
regulated medical waste must be stored,
collected, and treated. Providers of
infectious waste collection and
treatment services are required to be
licensed by the various state and
Federal regulatory agencies before they
can offer such services. Regulated
medical waste must be stored separately
from other types of waste, and each type
of regulated medical waste must be
stored separately from the other types in
specially marked and sealed containers.
Collection and transport to treatment
facilities must be performed by a stateapproved company.
State-approved treatment facilities
must be used to render regulated
medical waste non-infectious. Failure to
use state-approved treatment facilities
subjects both the generator of the
infectious waste and the infectious
waste collection and treatment service
provider to criminal prosecution, fines,
damage actions, and potentially high
clean-up costs.
Autoclaves are the most prevalent
treatment technology for infectious
waste. An autoclave uses steam
sterilization combined with pressure to
render infectious waste non-infectious.
Because autoclaving is a reliable and
long-proven technology for treating
infectious waste, it has become the
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preferred choice for treating infectious
waste.
The infectious waste collection and
treatment services industry categorizes
customers according to the amount of
infectious waste that they generate. LQG
customers typically are hospitals, large
laboratories, and other large medical
facilities that generate large amounts of
infectious waste. LQG customers often
need collection to occur on a daily
basis, or at least several times a week,
and must receive continuous supplies of
containers with sizeable storage
capacity from their service providers.
LQG customers require that their
service providers perform both
infectious waste collection and
treatment. They also require their
providers to meet strict standards to
ensure they have sufficient technical
capability, knowledge, and financial
resources. For example, LQG customers
typically require an infectious waste
collection and treatment service
provider to have: (a) An adequate
infrastructure to serve the customer’s
needs, including trucks, storage
containers, transfer stations, electronic
equipment capable of monitoring and
tracking each type of waste, and
personnel with a variety of expertise to
support the infrastructure; (b) an
established reputation for providing
reliable and timely collection and
treatment for LQG customers; (c) its own
infectious waste treatment facility to
minimize the number of companies that
handle the waste, thereby reducing the
possibility that the waste is mishandled;
and (d) substantial liability insurance
that meets all Federal and State
regulatory requirements governing
infectious waste.
Collection and treatment service
providers bid for each LQG customer’s
business separately, and an infectious
waste collection and treatment service
provider can identify the specific
competitive conditions that apply to
each LQG customer, including which
potential competitors can serve that
LQG customer. Infectious waste
collection and treatment service
providers for LQG customers can and do
price discriminate based on an LQG
customer’s requirements and the
number of competitors available to
provide such services.
A small but significant increase in the
price of infectious waste collection and
treatment services for LQG customers
would not cause LQG customers to
move sufficient volumes of infectious
waste to another type of collection and
treatment service so as to make such a
price increase unprofitable.
Accordingly, the provision of infectious
waste collection and treatment services
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for LQG customers is a line of commerce
and a relevant price discrimination
service market within the meaning of
Section 7 of the Clayton Act.
2. Relevant Geographic Market
The geographic market for the
provision of infectious waste collection
and treatment services for LQG
customers is largely defined by
transportation costs. Infectious waste
collection and treatment service
companies rely on trucks to transport
waste from customer sites to their
treatment facilities. Transfer stations
enable service providers to transfer their
waste into tractor-trailers and more costeffectively transport their waste to
treatment facilities. Typically, the
greater the distance between an LQG
customer’s operations and the service
provider’s treatment or transfer facility,
the less price competitive the provider
is.
For LQG customers served by
MedServe in Kansas, Missouri,
Nebraska, and Oklahoma, the only
competitive alternative is Stericycle. In
these states, no other infectious waste
collection and treatment service
provider has a facility located within
approximately 300 miles of Stericycle’s
or MedServe’s facilities.
In the states of Kansas, Missouri,
Nebraska, and Oklahoma, LQG
customers would not switch to a more
distant infectious waste collection and
treatment service provider in sufficient
numbers so as to make a small but
significant increase in price
unprofitable. Accordingly, the states of
Kansas, Missouri, Nebraska, and
Oklahoma are a relevant geographic
market within the meaning of Section 7
of the Clayton Act.
3. Anticompetitive Effects of the
Acquisition
In the states of Kansas, Missouri,
Nebraska, and Oklahoma, the market for
the provision of infectious waste
collection and treatment services for
LQG customers is highly concentrated.
Following the acquisition, Stericycle
would become the monopoly provider
of infectious waste collection and
treatment services for LQG customers in
these states.
Vigorous price competition between
Stericycle and MedServe in the
provision of infectious waste collection
and treatment services has benefited
LQG customers in Kansas, Missouri,
Nebraska, and Oklahoma. Stericycle and
MedServe are each other’s only rival,
directly competing on price and quality
of service in the provision of infectious
waste collection and treatment services
for LQG customers.
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Therefore, the proposed acquisition
will eliminate the competition between
Stericycle and MedServe; reduce the
number of providers of infectious waste
collection and treatment services for
LQG customers from two to one; and
enable Stericycle to establish a
monopoly in the provision of such
services, leading to higher prices and
lower quality of service for LQG
customers in Kansas, Missouri,
Nebraska, and Oklahoma, in violation of
Section 7 of the Clayton Act.
Successful entry into the provision of
infectious waste collection and
treatment services for LQG customers in
Kansas, Missouri, Nebraska, and
Oklahoma would be difficult, timeconsuming, and costly. A prospective
provider of infectious waste collection
and treatment services for LQG
customers faces substantial financial
and permitting requirements to build a
facility and the infrastructure needed to
serve LQG customers. It also must have
an established reputation for handling
large amounts of infectious waste
produced by LQG customers. A provider
of infectious waste collection and
treatment services for LQG customers in
Kansas, Missouri, Nebraska, and
Oklahoma must establish a treatment
facility that contains a treatment
technology, such as an autoclave, with
sufficient capacity for treating large
volumes of infectious waste. In addition
to the capital costs of the treatment unit,
local zoning and state permits are
required.
A provider of infectious waste
collection and treatment services for
LQG customers also must have an
infrastructure of trucks, transfer
stations, and electronic equipment
capable of collecting, transporting,
treating and disposing, and monitoring
and tracking the infectious waste. A
provider of infectious waste collection
and treatment services for LQG
customers also must develop a
reputation and record of reliably
collecting and treating large volumes of
infectious waste in compliance with
state and Federal regulations. In
addition, a provider of infectious waste
collection and treatment services for
LQG customers must have the financial
capability to indemnify LQG customers
for any environmental fines or accidents
resulting from the collection,
transportation, and treatment of the
infectious waste.
Obtaining the necessary permits and
building an autoclave facility,
establishing the infrastructure to serve
LQG customers, and developing a
reputation and record of service and
compliance would require in excess of
two years. Entry into the provision of
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infectious waste collection and
treatment services for LQG customers in
Kansas, Missouri, Nebraska, and
Oklahoma would not be timely, likely,
or sufficient to counter anticompetitive
price increases or diminished quality of
service that Stericycle could impose
after the proposed acquisition.
III. Explanation of the Proposed Final
Judgment
The terms of the proposed Final
Judgment will eliminate the
anticompetitive effects of the
acquisition alleged in the Complaint.
Section IV of the proposed Final
Judgment requires defendants, within
ninety (90) days after the filing of the
Complaint, or five (5) days after notice
of the entry of the Final Judgment by the
Court, whichever is later, to divest the
assets currently used by MedServe in
the provision of infectious waste
collection and treatment services to
LQG customers in Kansas, Missouri,
Nebraska, and Oklahoma to an acquirer
acceptable to the United States, in its
sole discretion. The assets to be
divested, along with associated tangible
and intangible assets, are MedServe’s
Newton, Kansas autoclave facility and
MedServe’s transfer stations in Kansas
City, Kansas; Oklahoma City, Oklahoma;
Omaha, Nebraska; and Booneville,
Missouri. These assets comprise all of
the assets used by MedServe in the
provision of infectious waste collection
and treatment services for LQG
customers in Kansas, Missouri,
Nebraska, and Oklahoma. The
divestiture of these assets according to
the terms of the proposed Final
Judgment will establish a new,
independent, and economically viable
competitor, thereby preserving
competition in the provision of
infectious waste collection and
treatment services for LQG customers in
Kansas, Missouri, Nebraska, and
Oklahoma.
In the event that defendants do not
accomplish the divestiture within the
time prescribed in the proposed Final
Judgment, the proposed Final Judgment
provides that the Court will appoint a
trustee selected by the United States to
effect the divestitures. If a trustee is
appointed, the proposed Final Judgment
provides that defendants will pay all
costs and expenses of the trustee. The
trustee’s commission will be structured
so as to provide an incentive for the
trustee based on the price obtained and
the speed with which the divestitures
are accomplished. After his or her
appointment becomes effective, the
trustee will file monthly reports with
the Court, United States, and the States
as appropriate, setting forth his or her
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efforts to accomplish the divestitures. At
the end of six months, if the divestitures
have not been accomplished, the
trustee, the United States, and the
States, will make recommendations to
the Court, which shall enter such orders
as appropriate in order to carry out the
purpose of the trust, including
extending the trust or the term of the
trustee’s appointment.
Section VII of the proposed Final
Judgment requires that defendants
provide advance notification of certain
future proposed acquisitions not
otherwise subject to the Hart-ScottRodino Antitrust Improvements Act of
1976, 15 U.S.C. 18a. That provision
requires 30 days’ advance written notice
to the United States and the States
before defendants acquire, directly or
indirectly, (1) any interest in any
business located in Kansas, Missouri,
Nebraska, and Oklahoma that is engaged
in the collection and treatment of
infectious waste; (2) other than in the
ordinary course of business, any assets
located in Kansas, Missouri, Nebraska,
and Oklahoma that are used in the
collection and treatment of infectious
waste; or (3) capital stock or voting
securities of any person that, at any time
during the twelve (12) months
immediately preceding such
acquisition, was engaged in the
collection and treatment of infectious
waste in Kansas, Missouri, Nebraska,
and Oklahoma, where that person’s
annual revenues in these states from the
collection and treatment of infectious
waste were in excess of $500,000. With
this provision, the United States and the
States will have knowledge in advance
of acquisitions that may impact
competition in the provision of
infectious waste collection and
treatment services for LQG customers in
Kansas, Missouri, Nebraska, and
Oklahoma.
IV. Remedies Available to Potential
Private Litigants
Section 4 of the Clayton Act (15
U.S.C. 15) provides that any person who
has been injured as a result of conduct
prohibited by the antitrust laws may
bring suit in Federal court to recover
three times the damages the person has
suffered, as well as costs and reasonable
attorneys’ fees. Entry of the proposed
Final Judgment will neither impair nor
assist the bringing of any private
antitrust damage action. Under the
provisions of Section 5(a) of the Clayton
Act (15 U.S.C. 16(a)), the proposed Final
Judgment has no prima facie effect in
any subsequent private lawsuit that may
be brought against the defendants.
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V. Procedures Available for
Modification of the Proposed Final
Judgment
The United States, the States, and the
defendants have stipulated that the
proposed Final Judgment may be
entered by the Court after compliance
with the provisions of the APPA,
provided that the United States has not
withdrawn its consent. The APPA
conditions entry upon the Court’s
determination that the proposed Final
Judgment is in the public interest. The
APPA provides a period of at least sixty
(60) days preceding the effective date of
the proposed Final Judgment within
which any person may submit to the
United States written comments
regarding the proposed Final Judgment.
Any person who wishes to comment
should do so within sixty (60) days of
the date of publication of this
Competitive Impact Statement in the
Federal Register, or the last date of
publication in a newspaper of the
summary of this Competitive Impact
Statement, whichever is later. All
comments received during this period
will be considered by the United States
Department of Justice, which remains
free to withdraw its consent to the
proposed Final Judgment at any time
prior to the Court’s entry of judgment.
The comments and the response of the
United States will be filed with the
Court and published in the Federal
Register.
Written comments should be
submitted to: Maribeth Petrizzi, Chief,
Litigation II Section, Antitrust Division,
United States Department of Justice, 450
Fifth Street, NW., Suite 8700,
Washington, DC 20530.
The proposed Final Judgment
provides that the Court retains
jurisdiction over this action, and the
parties may apply to the Court for any
order necessary or appropriate for the
modification, interpretation, or
enforcement of the Final Judgment.
VI. Alternatives to the Proposed Final
Judgment
The United States considered, as an
alternative to the proposed Final
Judgment, a full trial on the merits
against defendants. The United States
could have commenced litigation and
sought a judicial order enjoining the
acquisition of MedServe by Stericycle.
The United States is satisfied that the
divestiture and other relief described in
the proposed Final Judgment will
preserve competition in the provision of
infectious waste collection and
treatment services for LQG customers in
Kansas, Missouri, Nebraska, and
Oklahoma. The relief contained in the
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proposed Final Judgment would achieve
all or substantially all of the relief that
the United States would have obtained
through litigation, while avoiding the
time, expense, and uncertainty of a full
trial on the merits of the Complaint.
VII. Standard of Review Under the
APPA for the Proposed Final Judgment
The Clayton Act, as amended by the
APPA, requires that proposed consent
judgments in antitrust cases brought by
the United States be subject to a sixtyday comment period, after which the
court shall determine whether entry of
the Final Judgment ‘‘is in the public
interest.’’ 15 U.S.C. 16(e)(1). In making
that determination, in accordance with
the statute, the court is required to
consider:
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(A) The competitive impact of such
judgment, including termination of alleged
violations, provisions for enforcement and
modification, duration of relief sought,
anticipated effects of alternative remedies
actually considered, whether its terms are
ambiguous, and any other competitive
considerations bearing upon the adequacy of
such judgment that the court deems
necessary to a determination of whether the
consent judgment is in the public interest;
and
(B) the impact of entry of such judgment
upon competition in the relevant market or
markets, upon the public generally and
individuals alleging specific injury from the
violations set forth in the complaint
including consideration of the public benefit,
if any, to be derived from a determination of
the issues at trial.
15 U.S.C. 16(e)(1)(A)–(B). In
considering these statutory factors, the
court’s inquiry is necessarily a limited
one as the government is entitled to
‘‘broad discretion to settle with the
defendant within the reaches of the
public interest.’’ United States v.
Microsoft Corp., 56 F.3d 1448, 1461
(D.C. Cir. 1995); see generally United
States v. SBC Commc’ns, Inc., 489 F.
Supp. 2d 1 (D.D.C. 2007) (assessing
public interest standard under the
Tunney Act); United States v. InBev
N.V./S.A. 2009–2 Trade Cas. (CCH)
¶76,736, 2009 U.S. Dist. LEXIS 84787,
No. 08–1965 (JR), at *3 (D.D.C. Aug. 11,
2009) (noting that the court’s review of
a consent judgment is limited and only
inquires ‘‘into whether the government’s
determination that the proposed
remedies will cure the antitrust
violations alleged in the complaint was
reasonable, and whether the mechanism
to enforce the final judgment are clear
and manageable.’’).
As the United States Court of Appeals
for the District of Columbia has held,
under the APPA, a court considers,
among other things, the relationship
between the remedy secured and the
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specific allegations set forth in the
government’s complaint, whether the
decree is sufficiently clear, whether
enforcement mechanisms are sufficient,
and whether the decree may positively
harm third parties. See Microsoft, 56
F.3d at 1458–62. With respect to the
adequacy of the relief secured by the
decree, a court may not ‘‘engage in an
unrestricted evaluation of what relief
would best serve the public.’’ United
States v. BNS, Inc., 858 F.2d 456, 462
(9th Cir. 1988) (citing United States v.
Bechtel Corp., 648 F.2d 660, 666 (9th
Cir. 1981)); see also Microsoft, 56 F.3d
at 1460–62; United States v. Alcoa, Inc.,
152 F. Supp. 2d 37, 40 (D.D.C. 2001);
InBev, 2009 U.S. Dist. LEXIS 84787, at
*3. Courts have held that:
[T]he balancing of competing social and
political interests affected by a proposed
antitrust consent decree must be left, in the
first instance, to the discretion of the
Attorney General. The court’s role in
protecting the public interest is one of
insuring that the government has not
breached its duty to the public in consenting
to the decree. The court is required to
determine not whether a particular decree is
the one that will best serve society, but
whether the settlement is ‘‘within the reaches
of the public interest.’’ More elaborate
requirements might undermine the
effectiveness of antitrust enforcement by
consent decree.
Bechtel, 648 F.2d at 666 (emphasis
added) (citations omitted).1 In
determining whether a proposed
settlement is in the public interest, the
court ‘‘must accord deference to the
government’s predictions about the
efficacy of its remedies, and may not
require that the remedies perfectly
match the alleged violations.’’ SBC
Commc’ns, 489 F. Supp. 2d at 17; see
also Microsoft, 56 F.3d at 1461 (noting
the need for courts to be ‘‘deferential to
the government’s predictions as to the
effect of the proposed remedies’’);
United States v. Archer-DanielsMidland Co., 272 F. Supp. 2d 1, 6
(D.D.C. 2003) (noting that the court
should grant due respect to the United
States’ prediction as to the effect of
proposed remedies, its perception of the
market structure, and its views of the
nature of the case).
Courts have greater flexibility in
approving proposed consent decrees
1 Cf. BNS, 858 F.2d at 464 (holding that the
court’s ‘‘ultimate authority under the [APPA] is
limited to approving or disapproving the consent
decree’’); United States v. Gillette Co., 406 F. Supp.
713, 716 (D. Mass. 1975) (noting that, in this way,
the court is constrained to ‘‘look at the overall
picture not hypercritically, nor with a microscope,
but with an artist’s reducing glass’’). See generally
Microsoft, 56 F.3d at 1461 (discussing whether ‘‘the
remedies [obtained in the decree are] so
inconsonant with the allegations charged as to fall
outside of the ‘reaches of the public interest’ ’’).
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than in crafting their own decrees
following a finding of liability in a
litigated matter. ‘‘[A] proposed decree
must be approved even if it falls short
of the remedy the court would impose
on its own, as long as it falls within the
range of acceptability or is ‘within the
reaches of public interest.’ ’’ United
States v. Am. Tel. & Tel. Co., 552 F.
Supp. 131, 151 (D.D.C. 1982) (citations
omitted) (quoting United States v.
Gillette Co., 406 F. Supp. 713, 716 (D.
Mass. 1975)), aff’d sub nom. Maryland
v. United States, 460 U.S. 1001 (1983);
see also United States v. Alcan
Aluminum Ltd., 605 F. Supp. 619, 622
(W.D. Ky. 1985) (approving the consent
decree even though the court would
have imposed a greater remedy).
Therefore, the United States ‘‘need only
provide a factual basis for concluding
that the settlements are reasonably
adequate remedies for the alleged
harms.’’ SBC Commc’ns, 489 F. Supp. 2d
at 17.
Moreover, the court’s role under the
APPA is limited to reviewing the
remedy in relationship to the violations
that the United States has alleged in its
Complaint, and does not authorize the
court to ‘‘construct [its] own
hypothetical case and then evaluate the
decree against that case.’’ Microsoft, 56
F.3d at 1459; see also InBev, 2009 U.S.
Dist. LEXIS 84787, at *20 (‘‘the ‘public
interest’ is not to be measured by
comparing the violations alleged in the
complaint against those the court
believes could have, or even should
have, been alleged’’). Because the
‘‘court’s authority to review the decree
depends entirely on the government’s
exercising its prosecutorial discretion by
bringing a case in the first place,’’ it
follows that ‘‘the court is only
authorized to review the decree itself,’’
and not to ‘‘effectively redraft the
complaint’’ to inquire into other matters
that the United States did not pursue.
Microsoft, 56 F.3d at 1459–60. As this
Court confirmed in SBC
Communications, courts ‘‘cannot look
beyond the complaint in making the
public interest determination unless the
complaint is drafted so narrowly as to
make a mockery of judicial power.’’ 489
F. Supp. 2d at 15.
In its 2004 amendments to the
Tunney Act,2 Congress made clear its
2 The 2004 amendments substituted the word
‘‘shall’’ for ‘‘may’’ when directing the courts to
consider the enumerated factors and amended the
list of factors to focus on competitive considerations
and address potentially ambiguous judgment terms.
Compare 15 U.S.C. 16(e) (2004), with 15 U.S.C.
16(e)(1)(2006); see also SBC Commc’ns, 489 F.
Supp. 2d at 11 (concluding that the 2004
amendments ‘‘effected minimal changes’’ to Tunney
Act review.).
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intent to preserve the practical benefits
of utilizing consent decrees in antitrust
enforcement, stating: ‘‘[n]othing in this
section shall be construed to require the
court to conduct an evidentiary hearing
or to require the court to permit anyone
to intervene.’’ 15 U.S.C. 16 (e)(2). The
language wrote into the statute is what
Congress intended when it enacted the
Tunney Act in 1974, as Senator Tunney
explained: ‘‘[t]he court is nowhere
compelled to go to trial or to engage in
extended proceedings which might have
the effect of vitiating the benefits of
prompt and less costly settlement
through the consent decree process.’’
119 Cong. Rec. 24,598 (1973) (statement
of Senator Tunney). Rather, the
procedure for the public interest
determination is left to the discretion of
the court, with the recognition that the
court’s ‘‘scope of review remains sharply
proscribed by precedent and the nature
of Tunney Act proceedings.’’ SBC
Commc’ns, 489 F. Supp. 2d at 11.3
VIII. Determinative Documents
There are no determinative materials
or documents within the meaning of the
APPA that were considered by the
United States in formulating the
proposed Final Judgment.
Dated: January __ , 2010.
Respectfully submitted,
Frederick H. Parmenter,
U.S. Department of Justice, Antitrust
Division, Lit II Section, 450 Fifth Street,
NW., Suite 8700, Washington, DC 20530,
202–307–0620.
Certificate of Service
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I, Frederick H. Parmenter, hereby
certify that on January __ , 2010, caused
a copy of the foregoing Competitive
Impact Statement to be served upon
defendants Stericycle, Inc., ATMW
Acquisition Corp., MedServe, Inc., and
Avista Capital Partners, L.P., and
plaintiffs the State of Missouri and State
of Nebraska by mailing the document
electronically to the duly authorized
legal representatives as follows:
3 See United States v. Enova Corp., 107 F. Supp.
2d 10, 17 (D.D.C. 2000) (noting that the ‘‘Tunney
Act expressly allows the court to make its public
interest determination on the basis of the
competitive impact statement and response to
comments alone’’); United States v. Mid-Am.
Dairymen, Inc., 1977–1 Trade Cas. (CCH) ¶ 61,508,
at 71,980 (W.D. Mo. 1977) (‘‘Absent a showing of
corrupt failure of the government to discharge its
duty, the Court, in making its public interest
finding, should * * * carefully consider the
explanations of the government in the competitive
impact statement and its responses to comments in
order to determine whether those explanations are
reasonable under the circumstances.’’); S. Rep. No.
93–298, 93d Cong., 1st Sess., at 6 (1973) (‘‘Where
the public interest can be meaningfully evaluated
simply on the basis of briefs and oral arguments,
that is the approach that should be utilized.’’).
VerDate Nov<24>2008
18:35 Jan 29, 2010
Jkt 220001
Counsel for Defendants Stericycle, Inc.,
and ATMW Acquisition Corp.
David A. Clanton, D.C. Bar # 376880,
Baker & McKenzie LLP, 815 Connecticut
Avenue, NW., Washington, DC 20006–
4078, Tel: (202) 452–7014, Fax: (202)
416–6929, E-mail:
david.a.clanton@bakernet.com.
Counsel for Defendants MedServe, Inc.
and Avista Capital Partners, L.P.
Sean F.X. Boland, D.C. Bar # 249318,
Howrey LLP, 1299 Pennsylvania
Avenue, NW., Washington, DC 20004–
2402, Tel: (202) 383–7122, Fax: (202)
318–8649, E-mail:
BolandS@howrey.com.
Counsel for Plaintiff State of Missouri
Anne E. Schneider, Assistant
Attorney General, State of Missouri,
P.O. Box 899, Jefferson City, MO 65102,
Tel: (573) 751–8455, Fax: (573) 751–
2041, E-mail: Anne.Schneider@
ago.mo.govmailto:nicole.
gordon@doj.ca.gov.
Counsel for Plaintiff State of Nebraska
Leslie C. Levy, Assistant Attorney
General, Nebraska Attorney General’s
Office, 2115 State Capital Building,
Lincoln, NE 68509, Tel.: (402) 471–
2683, Fax: (402) 471–4725, E-mail:
leslie.levy@nebraska.gov.
Frederick H. Parmenter, United States
Department of Justice, Antitrust
Division, Litigation II Section, 450 Fifth
Street, NW., Suite 8700, Washington,
DC 20530, Tel.: (202) 307–0620, Fax:
(202) 307–6583, E-mail:
frederick.parmenter@usdoj.gov.
[FR Doc. 2010–1959 Filed 1–29–10; 8:45 am]
BILLING CODE 4410–11–P
DEPARTMENT OF JUSTICE
Antitrust Division
United States v. Cameron International
Corp., et al.; Proposed Final Judgment
and Competitive Impact Statement
Notice is hereby given pursuant to the
Antitrust Procedures and Penalties Act,
15 U.S.C. 16(b)–(h), that a proposed
Final Judgment, Stipulation and
Competitive Impact Statement have
been filed with the United States
District Court for the District of
Columbia in United States v. Cameron
Int’l Corp., et al., No. 09–cv–02165–
RMC. On November 17, 2009, the
United States filed a Complaint alleging
that the proposed acquisition by
Cameron International Corporation
(‘‘Cameron’’) of NATCO Group Inc.
(‘‘NATCO’’) would violate Section 7 of
the Clayton Act, 15 U.S.C. 18. The
PO 00000
Frm 00100
Fmt 4703
Sfmt 4703
proposed Final Judgment, filed the same
time as the Complaint, requires
Cameron to divest certain tangible and
intangible assets related to the
development, production, sale, repair,
and service of customized electrostatic
desalters used in the downstream oil
refining industry, an option to purchase
either Cameron’s or NATCO’s pilot
plant, and a license to NATCO’s
intellectual property and other assets
primarily used in or necessary to the
development, production, sale, repair,
or service of downstream refinery
desalters that utilize dual frequency
transformers and AC/DC power
supplies.
Copies of the Complaint, proposed
Final Judgment, and Competitive Impact
Statement are available for inspection at
the Department of Justice, Antitrust
Division, Antitrust Documents Group,
450 Fifth Street, NW., Suite 1010,
Washington, DC 20530 (telephone: 202–
514–2481), on the Department of
Justice’s Web site at https://
www.usdoj.gov/atr, and at the Office of
the Clerk of the United States District
Court for the District of Columbia.
Copies of these materials may be
obtained from the Antitrust Division
upon request and payment of the
copying fee set by Department of Justice
regulations.
Public comment is invited within 60
days of the date of this notice. Such
comments, and responses thereto, will
be published in the Federal Register
and filed with the Court. Comments
should be directed to Maribeth Petrizzi,
Chief, Litigation II Section, Antitrust
Division, U.S. Department of Justice,
450 Fifth Street, NW., Suite 8700,
Washington, DC 20530 (telephone: 202–
307–0924).
Patricia A. Brink,
Deputy Director of Operations and Civil
Enforcement.
United States of America, Antitrust
Division, 450 5th Street, NW., Suite 8700,
Washington, DC 20530, Plaintiff, v. Cameron
International Corporation, 1333 West Loop
South, Suite 1700, Houston, TX 77027, and
NATCO Group Inc., 11210 Equity Drive,
Suite 100, Houston, TX 77041, Defendants.
Case No.: Case: 1:09–cv–02165.
Assigned To: Bates, John D.
Assign Date: 11/17/2009.
Description: Antitrust.
Complaint
The United States of America
(‘‘United States’’), acting under the
direction of the Attorney General of the
United States, brings this civil antitrust
action against defendants Cameron
International Corporation (‘‘Cameron’’)
and NATCO Group Inc. (‘‘NATCO’’) to
enjoin Cameron’s proposed acquisition
E:\FR\FM\01FEN1.SGM
01FEN1
Agencies
[Federal Register Volume 75, Number 20 (Monday, February 1, 2010)]
[Notices]
[Pages 5120-5132]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2010-1959]
-----------------------------------------------------------------------
DEPARTMENT OF JUSTICE
Antitrust Division
United States, et al. v. Stericycle, Inc., et al.; Proposed Final
Judgment and Competitive Impact Statement
Notice is hereby given pursuant to the Antitrust Procedures and
Penalties Act, 15 U.S.C. 16(b)-(h), that a proposed
[[Page 5121]]
Final Judgment and Competitive Impact Statement have been filed with
the United States District Court for the District of Columbia in United
States, et al. v. Stericycle, Inc., et al., Civil Action No. 1:09-cv-
02268. On November 30, 2009, the United States and the States of
Missouri and Nebraska filed a Complaint alleging that the proposed
acquisition by Stericycle, Inc. of MedServe, Inc. would violate Section
7 of the Clayton Act, 15 U.S.C. 18. The proposed Final Judgment, filed
the same time as the Complaint, requires Stericycle to divest all
MedServe assets used in the provision of infectious waste collection
and treatment services for Large Quantity Generator (``LQG'') customers
in the states of Kansas, Missouri, Nebraska, and Oklahoma. These assets
include an autoclave in Newton, Kansas; transfer stations in Kansas
City, Kansas; Oklahoma City, Oklahoma; Omaha, Nebraska; and Booneville,
Missouri; LQG customer contracts associated with these facilities; and
certain tangible and intangible assets. Copies of the Complaint,
proposed Final Judgment, and Competitive Impact Statement are available
for inspection at the Department of Justice, Antitrust Division,
Antitrust Documents Group, 450 Fifth Street, NW., Suite 1010,
Washington, DC 20530 (telephone: 202-514-2481), on the Department of
Justice's Web site at https://www.usdoj.gov/atr, and at the Office of
the Clerk of the United States District Court for the District of
Columbia. Copies of these materials may be obtained from the Antitrust
Division upon request and payment of a copying fee set by Department of
Justice regulations.
Public comment is invited within 60 days of the date of this
notice. Such comments, and responses thereto, will be published in the
Federal Register and filed with the Court. Comments should be directed
to Maribeth Petrizzi, Chief, Litigation II Section, Antitrust Division,
U.S. Department of Justice, 450 Fifth Street, NW., Suite 8700,
Washington, DC 20530 (telephone: 202-307-0924).
J. Robert Kramer II,
Director of Operations and Civil Enforcement.
United States District Court for the District of Columbia
----------------------------------------------------------------------------------------------------------------
----------------------------------------------------------------------------------------------------------------
UNITED STATES OF AMERICA, Department of CASE NO.: 1:09-cv-02268; JUDGE: John D. Bates; DECK TYPE: Antitrust;
Justice, Antitrust Division, 450 5th DATE STAMP: November 30, 2009.
Street, NW., Suite 8700, Washington, DC
20530; STATE OF MISSOURI, Office of the
Attorney General, P.O. Box 899, Jefferson
City, Missouri 65102; and STATE OF
NEBRASKA, Office of the Attorney General,
2115 State Capitol Building, Lincoln,
Nebraska 68509-8920, Plaintiffs, v.
STERICYCLE, INC., 28161 North Keith
Drive, Lake Forest, Illinois 60045; ATMW
ACQUISITION CORP., 28161 North Keith
Drive, Lake Forest, Illinois 60045;
MEDSERVE, INC., 6575 West Loop South,
Suite 145, Bellaire, Texas, 77401; and
AVISTA CAPITAL PARTNERS, L.P., 6575 West
Loop South, Suite 145, Bellaire, Texas
77401, Defendants.
----------------------------------------------------------------------------------------------------------------
Complaint
Plaintiff, the United States of America (``United States''), acting
under the direction of the Attorney General of the United States, and
plaintiffs, the State of Missouri and the State of Nebraska, acting
under the direction of their respective Attorneys General, bring this
civil antitrust action against defendants, Stericycle, Inc. and ATMW
Acquisition Corp. and MedServe, Inc. and Avista Capital Partners, L.P.
to enjoin Stericycle's proposed acquisition of MedServe and to obtain
other equitable relief. Plaintiffs complain and allege as follows:
I. Nature of the Action
1. Pursuant to an agreement and plan of merger dated May 9, 2009,
Stericycle intends to acquire all of the voting shares of MedServe in a
transaction valued at $185 million. Defendants Stericycle and MedServe
currently compete in the provision of infectious waste collection and
treatment services for large quantity generator (``LQG'') customers.
The resulting combination would create a monopoly in the provision of
infectious waste collection and treatment services for LQG customers in
the states of Missouri, Nebraska, Oklahoma, and Kansas.
2. The United States, the State of Missouri, and the State of
Nebraska bring this action to prevent the proposed acquisition because
it would substantially lessen competition in the provision of
infectious waste collection and treatment services for LQG customers in
the states of Kansas, Missouri, Nebraska, and Oklahoma, in violation of
Section 7 of the Clayton Act, 15 U.S.C. 18.
II. Jurisdiction and Venue
3. The United States brings this action under Section 15 of the
Clayton Act, as amended, 15 U.S.C. 4 and 25, to prevent and restrain
defendants from violating Section 7 of the Clayton Act, 15 U.S.C. 18.
The State of Missouri and the State of Nebraska bring this action under
Section 16 of the Clayton Act, 15 U.S.C. 26, to prevent and restrain
defendants from violating Section 7 of the Clayton Act, 15 U.S.C. 18.
The State of Missouri and the State of Nebraska, by and through their
respective Attorneys General, or other authorized officials, bring this
action in their sovereign capacities and as parens patriae on behalf of
the citizens, general welfare, and economy of each of their states.
4. Defendants collect and treat infectious waste generated by LQG
customers in the flow of interstate commerce. Defendants' activities in
collecting and treating infectious waste substantially affect
interstate commerce. The Court has jurisdiction over this action and
over the parties pursuant to 15 U.S.C. 22, and 28 U.S.C. 1331 and 1337.
5. Defendants transact business, and have consented to venue and
personal jurisdiction, in the District of Columbia. Venue is therefore
proper in this District under Section 12 of the Clayton Act, 15 U.S.C.
22 and 28 U.S.C. 1391(c).
III. The Defendants
6. Defendant Stericycle, Inc. is a Delaware corporation with its
principal place of business in Lake Forest, Illinois. Stericycle, a
multi-national company, is the largest provider of infectious waste
collection and treatment services in the United States, with operations
in nearly all of the contiguous 48 states, including 46 treatment
facilities and 80 transfer and collection sites. In 2008, Stericycle
reported total worldwide sales of approximately $1.1 billion, of which
approximately 78 percent were generated in the United States. ATMW
Acquisition Corp. is a corporation formed by Stericycle to facilitate
its acquisition of MedServe. Stericycle and ATMW hereinafter are
collectively referred to as Stericycle.
7. Defendant MedServe is a Delaware corporation with its principal
place of business in Bellaire, Texas. MedServe is the second-largest
provider of infectious waste collection and treatment services in the
United States, with operations in
[[Page 5122]]
25 states that include eight treatment facilities and 18 transfer and
collection sites. In 2008, MedServe had total revenues of about $35.6
million. Avista Capital Partners, L.P. is an entity formed by MedServe
to facilitate the acquisition of MedServe by Stericycle. MedServe and
Avista hereinafter are collectively referred to as MedServe.
IV. Trade and Commerce
A. The Relevant Service Market
8. Regulated medical waste is waste generated in the diagnosis,
treatment, or immunization of human beings or animals. There are
generally three types of regulated medical waste: (1) Infectious waste;
(2) pathological waste; and (3) trace chemotherapy waste. Infectious
waste is waste that has come into contact with bodily fluids and
``sharps'' waste, such as syringes and scalpels. Pathological waste is
anatomical parts, and trace chemotherapy waste is small amounts of
chemical compounds used to treat cancer patients and the equipment used
to administer the compounds. Infectious waste comprises approximately
90 percent of the regulated medical waste generated in the United
States.
9. State and Federal governments heavily regulate the collection
and treatment of regulated medical waste. They prescribe how each type
of regulated medical waste must be stored, collected, and treated.
Providers of infectious waste collection and treatment services are
required to be licensed by various state and Federal regulatory
agencies before they can offer such services.
10. Regulated medical waste must be stored separately from other
types of waste, and each type of regulated medical waste must be stored
separately from the other types in specially marked and sealed
containers. Collection and transport of regulated medical waste to
treatment facilities must be performed by state-approved companies.
11. State-approved treatment facilities must be used to render
regulated medical waste non-infectious. Failure to use state-approved
treatment facilities subjects both the generator of the infectious
waste and the infectious waste collection and treatment service
provider to criminal prosecution, fines, damage actions, and
potentially high clean-up costs.
12. Autoclaves are the most prevalent treatment technology for
infectious waste. An autoclave uses steam sterilization combined with
pressure to render infectious waste non-infectious. Because autoclaving
is a reliable and long-proven technology, it has become the preferred
choice for treating infectious waste.
13. The infectious waste collection and treatment services industry
categorizes customers according to the amount of infectious waste they
generate. LQG customers typically are hospitals, large laboratories,
and other large medical facilities that generate large amounts of
infectious waste. LQG customers often need collection to occur on a
daily basis, or at least several times a week, and must receive
continuous supplies of containers with sizeable storage capacity from
their service providers.
14. LQG customers require their service providers to perform both
infectious waste collection and treatment. They also require their
providers to meet strict standards to ensure they have sufficient
technical capability, knowledge, and financial resources. For example,
an LQG customer typically requires an infectious waste collection and
treatment service provider to have: (a) An adequate infrastructure to
serve the customer's needs, including trucks, storage containers,
transfer stations, electronic equipment capable of monitoring and
tracking each type of waste, and personnel with a variety of expertise
to support the infrastructure; (b) an established reputation for
providing reliable and timely collection and treatment for LQG
customers; (c) its own infectious waste treatment facility to minimize
the number of companies that handle the waste, thereby reducing the
possibility that the waste is mishandled; and (d) substantial liability
insurance that meets all Federal and state regulatory requirements
governing infectious waste.
15. Collection and treatment providers bid for each LQG customer's
business separately, and an infectious waste collection and treatment
service provider can identify the specific competitive conditions that
apply to each LQG customer, including which potential competitors can
serve that LQG customer. Infectious waste collection and treatment
service providers for LQG customers can and do price discriminate based
on an LQG customer's requirements and the number of other competitors
available to provide such services.
16. A small but significant increase in the price of infectious
waste collection and treatment services for LQG customers would not
cause LQG customers to move sufficient volumes of infectious waste to
another type of collection and treatment service so as to make such a
price increase unprofitable.
17. Accordingly, the provision of infectious waste collection and
treatment services for LQG customers is a line of commerce and a
relevant price discrimination service market within the meaning of
Section 7 of the Clayton Act.
B. The Relevant Geographic Market
18. The geographic market for the provision of infectious waste
collection and treatment services for LQG customers is largely defined
by transportation costs. Infectious waste collection and treatment
companies rely on trucks to transport waste from customer sites to
their treatment facilities. Transfer stations enable service providers
to transfer their waste into tractor-trailers and more cost-effectively
to transport their waste to treatment facilities. Typically, the
greater the distance between an LQG customer's operations and the
service provider's treatment or transfer facility, the less price
competitive the provider is.
19. For LQG customers served by MedServe in Kansas, Missouri,
Nebraska, and Oklahoma, the only competitive alternative is Stericycle.
In these states, no other infectious waste collection and treatment
service provider has a facility located within approximately 300 miles
of Stericycle's or MedServe's facilities.
20. In the states of Kansas, Missouri, Nebraska, and Oklahoma, LQG
customers would not switch to a more distant infectious waste
collection and treatment service provider in sufficient numbers so as
to make a small but significant increase in price unprofitable.
21. Accordingly, the states of Kansas, Missouri, Nebraska, and
Oklahoma are a relevant geographic market within the meaning of Section
7 of the Clayton Act.
C. Anticompetitive Effects of the Acquisition
22. In the states of Kansas, Missouri, Nebraska, and Oklahoma, the
market for the provision of infectious waste collection and treatment
services for LQG customers is highly concentrated. Following the
acquisition, Stericycle would become the monopoly provider of
infectious waste collection and treatment services for LQG customers in
these states.
23. Vigorous price competition between Stericycle and MedServe in
the provision of infectious waste collection and treatment services has
benefited LQG customers in Kansas, Missouri, Nebraska, and Oklahoma.
Stericycle and MedServe are each other's only rivals, directly
competing on price and quality
[[Page 5123]]
of service in the provision of infectious waste collection and
treatment services for LQG customers.
24. Therefore, the proposed acquisition will eliminate the
competition between Stericycle and MedServe; reduce the number of
providers of infectious waste collection and treatment services for LQG
customers from two to one; and enable Stericycle to establish a
monopoly in the provision of such services, leading to higher prices
and lower quality of service for LQG customers in Kansas, Missouri,
Nebraska, and Oklahoma, in violation of Section 7 of the Clayton Act.
D. Entry Into Collection and Treatment of Infectious Waste Generated by
LQG Customers
25. Successful entry into the provision of collection and treatment
services for infectious waste for LQG customers in Kansas, Missouri,
Nebraska, and Oklahoma would be difficult, time-consuming, and costly.
A prospective provider of infectious waste collection and treatment
services for LQG customers faces substantial financial and permitting
requirements to build a facility and the infrastructure needed to serve
LQG customers. It also must have an established reputation for handling
the large amounts of infectious waste produced by LQG customers.
26. A provider of infectious waste collection and treatment
services for LQG customers in Kansas, Missouri, Nebraska, and Oklahoma
must establish a treatment facility that contains a treatment
technology, such as an autoclave, with sufficient capacity for treating
large volumes of infectious waste. In addition to the capital costs of
the treatment unit, local zoning and state permits are required.
27. A provider of infectious waste collection and treatment
services for LQG customers also must have an infrastructure of trucks,
transfer stations, and electronic equipment capable of collecting,
transporting, treating and disposing, and monitoring and tracking the
infectious waste.
28. A provider of infectious waste collection and treatment
services for LQG customers must develop a reputation and record of
reliably collecting and treating large volumes of infectious waste in
compliance with state and Federal regulations.
29. A provider of infectious waste collection and treatment
services for LQG customers must have the financial capability to
indemnify LQG customers for any environmental fines or accidents
resulting from the collection, transportation, and treatment of the
infectious waste.
30. Obtaining the necessary permits and building an autoclave
facility, establishing the infrastructure to serve LQG customers, and
developing a reputation and record of service and compliance would
require in excess of two years.
31. Entry into the provision of infectious waste collection and
treatment services for LQG customers in Kansas, Missouri, Nebraska, and
Oklahoma would not be timely, likely, or sufficient to counter
anticompetitive price increases or diminished quality of service that
Stericycle could impose after the proposed acquisition.
V. Violation Alleged
32. The United States incorporates the allegations of paragraphs 1
through 31 above.
33. Stericycle's proposed acquisition of all of MedServe's voting
securities and infectious waste collection and treatment assets in the
states of Kansas, Missouri, Nebraska, and Oklahoma will substantially
lessen competition and tend to create a monopoly in interstate trade
and commerce in violation of Section 7 of the Clayton Act, 15 U.S.C.
18.
34. Unless restrained, the transaction will have the following
anticompetitive effects, among others:
a. Actual and potential competition between Stericycle and MedServe
in the provision of infectious waste collection and treatment services
for LQG customers in the states of Kansas, Missouri, Nebraska, and
Oklahoma will be eliminated;
b. Competition generally in the provision of infectious waste
collection and treatment services for LQG customers in the states of
Kansas, Missouri, Nebraska, and Oklahoma will be substantially
lessened; and
c. Prices for infectious waste collection and treatment services
for LQG customers in the states of Kansas, Missouri, Nebraska, and
Oklahoma will likely increase, and service likely will be reduced.
VI. Requested Relief
35. Plaintiffs request:
a. That Stericycle's proposed acquisition of MedServe be adjudged
and decreed to be unlawful and in violation of Section 7 of the Clayton
Act, 15 U.S.C. 18;
b. That defendants and all persons acting on their behalf be
permanently enjoined and restrained from consummating the proposed
acquisition of MedServe by Stericycle, or from entering into or
carrying out any contract, agreement, plan, or understanding, the
effect of which would be to merge the voting securities or assets of
the defendants;
c. That plaintiffs receive such other and further relief as the
case requires and the Court deems just and proper; and
d. That plaintiffs recover the costs of this action.
Dated: November 30, 2009.
Respectfully submitted,
For Plaintiff United States of America.
/s/--------------------------------------------------------------------
Christine A. Varney,
Assistant Attorney General, D.C. Bar # 435204.
/s/--------------------------------------------------------------------
Maribeth Petrizzi,
Chief, Litigation II Section.
/s/--------------------------------------------------------------------
Molly S. Boast,
Deputy Assistant Attorney General.
/s/--------------------------------------------------------------------
Dorothy B. Fountain,
Assistant Chief, Litigation II Section, D.C. Bar # 439469.
/s/--------------------------------------------------------------------
J. Robert Kramer II,
Director of Operations.
/s/--------------------------------------------------------------------
Frederick H. Parmenter
Stephen A. Harris
Carolyn Davis
Leslie D. Peritz
Jay D. Owen,
Attorneys. U.S. Department of Justice, Antitrust Division,
Litigation II Section, Suite 8700, 450 Fifth Street, NW.,
Washington, DC 20530. Tel: (202) 307-0924, Fax: (202) 307-6583, E-
mail: Frederick.Parmenter@usdoj.gov.
For Plaintiff State of Missouri.
Chris Koster,
Attorney General.
By:
/s/--------------------------------------------------------------------
Anne E. Schneider,
Assistant Attorney General, State of Missouri, P.O. Box 899,
Jefferson City, MO 65102, Tel: (573) 751-8455, Fax: (573) 751-2041,
E-mail: Anne.Schneider@ago.mo.gov.
For Plaintiff State of Nebraska.
Jon Bruning,
Attorney General.
By:
/s/--------------------------------------------------------------------
Leslie C. Levy,
Assistant Attorney General, 2115 State Capitol Building, Lincoln, NE
68509-8920, Tel.: (402) 471-2811, Fax: (402) 471-4725, E-mail:
Leslie.Levy@nebraska.gov.
IN THE UNITED STATES DISTRICT COURT FOR THE DISTRICT OF COLUMBIA
[[Page 5124]]
------------------------------------------------------------------------
------------------------------------------------------------------------
UNITED STATES OF AMERICA, STATE CASE NO.: 1:09-cv-02268, JUDGE: John
OF MISSOURI, and STATE OF D. Bates, DECK TYPE: Antitrust, DATE
NEBRASKA, Plaintiffs, v. STAMP: November 30, 2009.
STERICYCLE, INC., ATMW
ACQUISITION CORP., MEDSERVE,
INC., and AVISTA CAPITAL
PARTNERS, L.P., Defendants.
------------------------------------------------------------------------
Proposed Final Judgement
Whereas, plaintiffs, the United States of America, the State of
Missouri, and the State of Nebraska, filed their Complaint on November
30, 2009; plaintiffs and defendants, Stericycle, Inc. and ATMW
Acquisition Corp., and MedServe, Inc. and Avista Capital Partners,
L.P., by their respective attorneys, have consented to the entry of
this Final Judgment without trial or adjudication of any issue of fact
or law; and without this Final Judgment constituting any evidence
against or admission by any party regarding any issue of law or fact;
And Whereas, defendants agree to be bound by the provisions of this
Final Judgment pending its approval by the Court;
And Whereas, the essence of this Final Judgment is the prompt and
certain divestiture of the Divestiture Assets to assure that
competition is not substantially lessened;
And Whereas, the United States requires defendants to make certain
divestitures for the purpose of remedying the loss of competition
alleged in the Complaint;
And Whereas, defendants have represented to the United States that
the divestitures required below can and will be made, and that
defendants will later raise no claim of hardship or difficulty as
grounds for asking the Court to modify any of the divestiture
provisions contained below;
Now, Therefore, before any testimony is taken, without trial or
adjudication of any issue of fact or law, and upon consent of the
parties, it is hereby Ordered, Adjudged, and Decreed:
I. Jurisdiction
This Court has jurisdiction over the subject matter of and each of
the parties to this action. The Complaint states a claim upon which
relief may be granted against the defendants under Section 7 of the
Clayton Act, 15 U.S.C. 18, as amended.
II. Definitions
As used in this Final Judgment:
A. ``Acquirer'' means the entity to which defendants shall divest
the Divestiture Assets.
B. ``Stericycle'' means defendant Stericycle, Inc., a Delaware
corporation with its principal place of business in Lake Forest,
Illinois, and ATMW Acquisition Corp. (a corporation formed to
facilitate the acquisition), and their successors, assigns,
subsidiaries, divisions, groups, affiliates, partnerships, and joint
ventures, and all of their directors, officers, managers, agents, and
employees.
C. ``MedServe'' means defendant MedServe, Inc., a Delaware
corporation with its principal place of business in Bellaire, Texas,
and Avista Capital Partners, L.P. formed to facilitate the acquisition,
and their successors, assigns, subsidiaries, divisions, groups,
affiliates, partnerships, and joint ventures, and all of their
directors, officers, managers, agents, and employees.
D. ``Infectious Waste'' means regulated medical waste that is
generated in the diagnosis, treatment, or immunization of human beings
or animals and that has come into contact with bodily fluids, and
``sharps'' waste, such as syringes and scalpels.
E. ``Treatment'' means the sterilization of infectious waste at a
state-approved treatment facility, including the use of transfer
stations to facilitate the shipment of infectious waste to other
treatment sites.
F. ``Large Quantity Generator Customer'' or ``LQG Customer'' means
any customer that spends $1000 or more per month on infectious waste
collection and treatment services.
G. ``Divestiture Assets'' means:
1. The following facilities:
a. MedServe's Newton, Kansas autoclave facility, located at 1021
South Spencer Avenue, Newton, Kansas 67114;
b. MedServe's Kansas City, Kansas transfer station, located at 200
Funston Road, Suite B, Kansas City, Kansas 66115;
c. MedServe's Oklahoma City, Oklahoma transfer station, located at
8800 SW 8th Street, Oklahoma City, Oklahoma 73128;
d. MedServe's Omaha, Nebraska transfer station, located at 13824-C
Plaza, Omaha, Nebraska 68144; and
e. MedServe's Booneville, Missouri transfer station, located at 680
Al Bersted Drive, Booneville, Missouri 65233;
2. All tangible assets at the MedServe facilities listed in
Paragraph II(G)(1), including all research and development activities,
equipment, and fixed assets, real property (leased or owned),
equipment, personal property, inventory (containers), office furniture,
materials, supplies, on- or off-site warehouses or storage facilities;
all licenses, permits, and authorizations issued by any governmental
organization relating to the facilities; all lists of MedServe LQG
customers; all MedServe LQG customer contracts, accounts, and credit
records; all other records; and all trucks and other vehicles assigned
to the facilities as of May 9, 2009; and
3. All intangible assets associated with the MedServe facilities
listed in Paragraph II(G)(1), including, but not limited to, all
contractual rights, patents, licenses and sublicenses, intellectual
property, technical information, computer software (including waste
monitoring software and management information systems) and related
documentation, know-how, trade secrets, drawings, blueprints, designs,
design protocols, specifications for materials, specifications for
parts and devices, safety procedures for the handling of materials and
substances, quality assurance and control procedures, design tools and
simulation capability, all manuals and technical information provided
to employees, customers, suppliers, agents or licensees.
III. Applicability
A. This Final Judgment applies to Stericycle and MedServe, as
defined above, and all other persons in active concert or participation
with either of them, who receive actual notice of this Final Judgment
by personal service or otherwise.
B. If, prior to complying with Sections IV and V of this Final
Judgment, defendants sell or otherwise dispose of all or substantially
all of their assets or of lesser business units that include the
Divestiture Assets, they shall require the purchaser to be bound by the
provisions of this Final Judgment. Defendants need not obtain such an
agreement from the Acquirer of the assets divested pursuant to this
Final Judgment.
IV. Divestitures
A. Defendants are ordered and directed, within ninety (90) calendar
days after the filing of the Complaint in this matter, or five (5)
calendar days after notice of the entry of this Final Judgment by the
Court, whichever is
[[Page 5125]]
later, to divest the Divestiture Assets in a manner consistent with
this Final Judgment to an Acquirer acceptable to the United States in
its sole discretion, after consultation with the State of Missouri and
the State of Nebraska. The United States, in its sole discretion, after
consultation with the State of Missouri and the State of Nebraska, may
agree to one or more extensions of this time period not to exceed sixty
(60) calendar days in total, and shall notify the Court in such
circumstances. Defendants agree to use their best efforts to divest the
Divestiture Assets as expeditiously as possible.
B. In accomplishing the divestitures ordered by this Final
Judgment, defendants promptly shall make known, by usual and customary
means, the availability of the Divestiture Assets. Defendants shall
inform any person making an inquiry regarding a possible purchase of
the Divestiture Assets that they are being divested pursuant to this
Final Judgment and provide that person with a copy of this Final
Judgment. Defendants shall offer to furnish to all prospective
Acquirers, subject to customary confidentiality assurances, all
information and documents relating to the Divestiture Assets
customarily provided in a due diligence process except such information
or documents subject to the attorney-client privilege or work-product
doctrine. Defendants shall make available such information to the
United States at the same time that such information is made available
to any other person.
C. Defendants shall provide the Acquirer and the United States
information relating to the personnel involved in the operation and
management of the Divestiture Assets to enable the Acquirer to make
offers of employment. Defendants shall not interfere with any
negotiations by the Acquirer to employ or contract with any defendant
employee whose primary responsibility is the operation or management of
the Divestiture Assets.
D. Defendants shall permit prospective Acquirers of the Divestiture
Assets to have reasonable access to personnel and to make inspections
of the physical facilities of the Divestiture Assets; access to any and
all environmental, zoning, and other permit documents and information;
and access to any and all financial, operational or other documents and
information customarily provided as part of a due diligence process.
E. Defendants shall warrant to the Acquirer that each asset will be
operational on the date of sale.
F. Defendants shall not take any action that will impede in any way
the permitting, operation or divestiture of the Divestiture Assets.
G. Defendants shall warrant to the Acquirer that there are no
material defects in the environmental, zoning or other permits
pertaining to the operation of the Divestiture Assets, and that
following the sale of the Divestiture Assets, defendants will not
undertake, directly or indirectly, any challenges to the environmental,
zoning, or other permits relating to the operation of the Divestiture
Assets.
H. Unless the United States, after consultation with the State of
Missouri and the State of Nebraska, otherwise consents in writing, the
divestitures pursuant to Section IV, or by trustee appointed pursuant
to Section V, of this Final Judgment, shall be made to a single
Acquirer and shall include all the Divestiture Assets, and shall be
accomplished in such a way as to satisfy the United States, in its sole
discretion, after consultation with the State of Missouri and the State
of Nebraska, that the divestitures will achieve the purposes of this
Final Judgment and that the Divestiture Assets can and will be used by
the Acquirer as part of a viable, ongoing business providing infectious
waste collection and treatment services for LQG customers located in
Kansas, Missouri, Nebraska, and Oklahoma. The divestitures, whether
pursuant to Section IV or Section V of this Final Judgment:
1. Shall be made to the Acquirer that, in the United States's sole
judgment, after consultation with the State of Missouri and the State
of Nebraska, has the intent and capability (including the necessary
managerial, operational, technical and financial capability) of
competing effectively in the business of providing infectious waste
collection and treatment services for LQG customers; and
2. Shall be accomplished so as to satisfy the United States, in its
sole discretion, after consultation with the State of Missouri and the
State of Nebraska, that none of the terms of any agreement between the
Acquirer and defendants gives defendants the ability unreasonably to
raise the Acquirer's costs, to lower the Acquirer's efficiency, or
otherwise to interfere in the ability of the Acquirer to compete
effectively.
V. Appointment of Trustee
A. If defendants have not divested the Divestiture Assets within
the time period specified in Section IV, defendants shall notify the
United States of that fact in writing. Upon application of the United
States, the Court shall appoint a trustee selected by the United States
and approved by the Court to effect the sale of the Divestiture Assets.
B. After the appointment of a trustee becomes effective, only the
trustee shall have the right to sell the Divestiture Assets. The
trustee shall have the power and authority to accomplish the
divestitures to an Acquirer acceptable to the United States, after
consultation with the State of Missouri and the State of Nebraska, at
such price and on such terms as are then obtainable upon reasonable
effort by the trustee, subject to the provisions of Sections IV, V and
VI of this Final Judgment, and shall have such other powers as this
Court deems appropriate. Subject to Section V, Paragraph D, of this
Final Judgment, the trustee may hire at the defendants' cost and
expense any investment bankers, attorneys, or other agents, who shall
be solely accountable to the trustee, reasonably necessary in the
trustee's judgment to assist in the divestitures.
C. Defendants shall not object to a sale by the trustee on any
ground other than the trustee's malfeasance. Any such objections by
defendants must be conveyed in writing to the United States and the
trustee within ten (10) calendar days after the trustee has provided
the notice required under Section VI.
D. The trustee shall serve at the cost and expense of defendants,
on such terms and conditions as the United States approves, and shall
account for all monies derived from the sale of the assets sold by the
trustee and all costs and expenses so incurred. After approval by the
Court of the trustee's accounting, including fees for its services and
those of any professionals and agents retained by the trustee, all
remaining money shall be paid to defendants and the trust shall then be
terminated. The compensation of the trustee and any professionals and
agents retained by the trustee shall be reasonable in light of the
value of the Divestiture Assets and based on a fee arrangement
providing the trustee with an incentive based on the price and terms of
the divestitures and the speed with which it is accomplished, but
timeliness is paramount.
E. Defendants shall use their best efforts to assist the trustee in
accomplishing the required divestitures. The trustee and any
consultants, accountants, attorneys, and other persons retained by the
trustee shall have full and complete access to the personnel, books,
records, and facilities of the business to be divested, and defendants
shall develop financial and other information relevant to such business
as the trustee may reasonably request, subject to reasonable protection
for trade secret or other confidential
[[Page 5126]]
research, development, or commercial information. Defendants shall take
no action to interfere with or to impede the trustee's accomplishment
of the divestitures.
F. After its appointment, the trustee shall file monthly reports
with the United States, the State of Missouri, the State of Nebraska,
and the Court setting forth the trustee's efforts to accomplish the
divestitures ordered under this Final Judgment. To the extent such
reports contain information that the trustee deems confidential, such
reports shall not be filed in the public docket of the Court. Such
reports shall include the name, address, and telephone number of each
person who, during the preceding month, made an offer to acquire,
expressed an interest in acquiring, entered into negotiations to
acquire, or was contacted or made an inquiry about acquiring, any
interest in the Divestiture Assets, and shall describe in detail each
contact with any such person. The trustee shall maintain full records
of all efforts made to divest the Divestiture Assets.
G. If the trustee has not accomplished the divestitures ordered
under this Final Judgment within six (6) months after its appointment,
the trustee shall promptly file with the Court a report setting forth:
(1) The trustee's efforts to accomplish the required divestitures; (2)
the reasons, in the trustee's judgment, why the required divestitures
have not been accomplished; and (3) the trustee's recommendations. To
the extent such reports contain information that the trustee deems
confidential, such reports shall not be filed in the public docket of
the Court. The trustee shall at the same time furnish such report to
the United States, which shall have the right to make additional
recommendations consistent with the purpose of the trust. The Court
thereafter shall enter such orders as it shall deem appropriate to
carry out the purpose of the Final Judgment, which may, if necessary,
include extending the trust and the term of the trustee's appointment
by a period requested by the United States.
VI. Notice of Proposed Divestitures
A. Within two (2) business days following execution of a definitive
divestiture agreement, defendants or the trustee, whichever is then
responsible for effecting the divestitures required herein, shall
notify the United States, the State of Missouri, and the State of
Nebraska of any proposed divestiture required by Section IV or V of
this Final Judgment. If the trustee is responsible, it shall similarly
notify defendants. The notice shall set forth the details of the
proposed divestitures and list the name, address, and telephone number
of each person not previously identified who offered or expressed an
interest in or desire to acquire any ownership interest in the
Divestiture Assets, together with full details of the same.
B. Within fifteen (15) calendar days of receipt of such notice by
the United States, the State of Missouri, and the State of Nebraska,
the United States may request from defendants, the proposed Acquirer,
any other third party, or the trustee, if applicable, additional
information concerning the proposed divestitures, the proposed Acquirer
and any other potential Acquirer. Defendants and the trustee shall
furnish any additional information requested within fifteen (15)
calendar days of the receipt of the request, unless the parties shall
otherwise agree.
C. Within thirty (30) calendar days after receipt of the notice or
within twenty (20) calendar days after the United States has been
provided the additional information requested from defendants, the
proposed Acquirer, any third party, and the trustee, whichever is
later, the United States shall provide written notice to defendants and
the trustee, if there is one, stating whether or not it objects to the
proposed divestitures. If the United States, after consultation with
the State of Missouri and the State of Nebraska, provides written
notice that it does not object, the divestitures may be consummated,
subject only to defendants' limited right to object to the sale under
paragraph V(C) of this Final Judgment. Absent written notice that the
United States does not object to the proposed Acquirer or upon
objection by the United States, a divestiture proposed under Section IV
or Section V shall not be consummated. Upon objection by defendants
under paragraph V(C), a divestiture proposed under Section V shall not
be consummated unless approved by the Court.
VII. Notice of Future Acquisitions
A. Unless such transaction is otherwise subject to the reporting
and waiting period requirements of the Hart-Scott-Rodino Antitrust
Improvements Act of 1976, as amended, 15 U.S.C. 18a (the ``HSR Act''),
Stericycle, without providing advance notification to the United
States, the State of Missouri, and the State of Nebraska, shall not
directly or indirectly acquire, any (1) interest in any business
located in Kansas, Missouri, Nebraska, and Oklahoma that is engaged in
the collection and treatment of infectious waste; (2) other than in the
ordinary course of business, assets located in Kansas, Missouri,
Nebraska, and Oklahoma that are used in the collection and treatment of
infectious waste; or (3) capital stock or voting securities of any
person that, at any time during the twelve (12) months immediately
preceding such acquisition, was engaged in the collection and treatment
of infectious waste in Kansas, Missouri, Nebraska, or Oklahoma, where
that person's annual revenues in these states from the collection and
treatment of infectious waste were in excess of $500,000.
B. Such notification shall be provided to the United States, the
State of Missouri, and the State of Nebraska in the same format as, and
per the instructions relating to the Notification and Report Form set
forth in the Appendix to Part 803 of Title 16 of the Code of Federal
Regulations as amended, except that the information requested in Items
5 through 9 of the instructions must be provided only about the
collection and treatment of infectious waste. Notification shall be
provided at least thirty (30) calendar days prior to acquiring any such
interest, and shall include, beyond what may be required by the
applicable instructions, the names of the principal representatives of
the parties to the agreement who negotiated the agreement, and any
management or strategic plans discussing the proposed transaction. If
within the 30-day period after notification, representatives of the
United States make a written request for additional information,
Stericycle shall not consummate the proposed transaction or agreement
until thirty (30) calendar days after submitting all such additional
information. Early termination of the waiting periods in this paragraph
may be requested and, where appropriate, granted in the same manner as
is applicable under the requirements and provisions of the HSR Act and
rules promulgated thereunder. This Section shall be broadly construed
and any ambiguity or uncertainty regarding the filing of notice under
this Section shall be resolved in favor of filing notice.
VIII. Financing
Defendants shall not finance all or any part of any purchase made
pursuant to Section IV or V of this Final Judgment.
IX. Hold Separate
Until the divestitures required by this Final Judgment have been
accomplished, defendants shall take all steps necessary to comply with
the Hold Separate Stipulation and Order entered by this Court.
Defendants shall take no
[[Page 5127]]
action that would jeopardize the divestitures ordered by this Court.
X. Affidavits
A. Within twenty (20) calendar days of the filing of the Complaint
in this matter, and every thirty (30) calendar days thereafter until
the divestitures have been completed under Section IV or V, defendants
shall deliver to the United States, the State of Missouri, and the
State of Nebraska an affidavit as to the fact and manner of its
compliance with Section IV or V of this Final Judgment. Each such
affidavit shall include the name, address, and telephone number of each
person who, during the preceding thirty (30) calendar days, made an
offer to acquire, expressed an interest in acquiring, entered into
negotiations to acquire, or was contacted or made an inquiry about
acquiring, any interest in the Divestiture Assets, and shall describe
in detail each contact with any such person during that period. Each
such affidavit shall also include a description of the efforts
defendants have taken to solicit buyers for the Divestiture Assets, and
to provide required information to prospective Acquirers, including the
limitations, if any, on such information. Assuming the information set
forth in the affidavit is true and complete, any objection by the
United States, after consultation with the State of Missouri and the
State of Nebraska, to information provided by defendants, including
limitation on information, shall be made within fourteen (14) calendar
days of receipt of such affidavit.
B. Within twenty (20) calendar days of the filing of the Complaint
in this matter, defendants shall deliver to the United States an
affidavit that describes in reasonable detail all actions defendants
have taken and all steps defendants have implemented on an ongoing
basis to comply with Section IX of this Final Judgment. Defendants
shall deliver to the United States, the State of Missouri, and the
State of Nebraska, an affidavit describing any changes to the efforts
and actions outlined in defendants' earlier affidavits filed pursuant
to this section within fifteen (15) calendar days after the change is
implemented.
C. Defendants shall keep all records of all efforts made to
preserve and divest the Divestiture Assets until one year after such
divestitures have been completed.
XI. Compliance Inspection
A. For the purposes of determining or securing compliance with this
Final Judgment, or of determining whether the Final Judgment should be
modified or vacated, and subject to any legally recognized privilege,
from time to time authorized representatives of the United States
Department of Justice Antitrust Division (``DOJ''), including
consultants and other persons retained by the United States, shall,
upon written request of an authorized representative of the Assistant
Attorney General in charge of the Antitrust Division, and on reasonable
notice to defendants, be permitted:
1. access during defendants' office hours to inspect and copy, or
at the option of the United States, to require defendants to provide
hard copy or electronic copies of, all books, ledgers, accounts,
records, data, and documents in the possession, custody, or control of
defendants, relating to any matters contained in this Final Judgment;
and
2. to interview, either informally or on the record, defendants'
officers, employees, or agents, who may have their individual counsel
present, regarding such matters. The interviews shall be subject to the
reasonable convenience of the interviewee and without restraint or
interference by defendants.
B. Upon the written request of an authorized representative of the
Assistant Attorney General in charge of the Antitrust Division,
defendants shall submit written reports or responses to written
interrogatories, under oath if requested, relating to any of the
matters contained in this Final Judgment as may be requested.
C. No information or documents obtained by the means provided in
this section shall be divulged by the United States to any person other
than an authorized representative of the executive branch of the United
States, except in the course of legal proceedings to which the United
States is a party (including grand jury proceedings), or for the
purpose of securing compliance with this Final Judgment, or as
otherwise required by law.
D. If at the time information or documents are furnished by
defendants to the United States, defendants represent and identify in
writing the material in any such information or documents to which a
claim of protection may be asserted under Rule 26(c)(1)(G) of the
Federal Rules of Civil Procedure, and defendants mark each pertinent
page of such material, ``Subject to claim of protection under Rule
26(c)(1)(G) of the Federal Rules of Civil Procedure,'' then the United
States shall give defendants ten (10) calendar days notice prior to
divulging such material in any legal proceeding (other than a grand
jury proceeding).
XII. No Reacquisition
During the term of this Final Judgment, defendants may not
reacquire any part of the Divestiture Assets, nor may any defendant
participate in any other transaction that would result in a
combination, merger, or other joining together of any part of the
Divestiture Assets with assets of the divesting company.
XIII. Retention of Jurisdiction
This Court retains jurisdiction to enable any party to this Final
Judgment to apply to this Court at any time for further orders and
directions as may be necessary or appropriate to carry out or construe
this Final Judgment, to modify any of its provisions, to enforce
compliance, and to punish violations of its provisions.
XIV. Expiration of Final Judgment
Unless this Court grants an extension, this Final Judgment shall
expire ten (10) years from the date of its entry.
XV. Public Interest Determination
Entry of this Final Judgment is in the public interest. The parties
have complied with the requirements of the Antitrust Procedures and
Penalties Act, 15 U.S.C. 16, including making copies available to the
public of this Final Judgment, the Competitive Impact Statement, and
any comments thereon and the United States's responses to comments.
Based upon the record before the Court, which includes the Competitive
Impact Statement and any comments and response to comments filed with
the Court, entry of this Final Judgment is in the public interest.
Date:------------------------------------------------------------------
Court approval subject to procedures of Antitrust Procedures and
Penalties Act, 15 U.S.C. 16
-----------------------------------------------------------------------
United States District Judge
United States District Court for the District of Columbia
[[Page 5128]]
------------------------------------------------------------------------
------------------------------------------------------------------------
UNITED STATES CASE NO.: 1:09-cv-02268, JUDGE: Hon.
OF AMERICA, John D. Bates, DECK TYPE: Antitrust,
STATE OF DATE STAMP.
MISSOURI, and
STATE OF
NEBRASKA,
Plaintiffs, v.
STERICYCLE,
INC., ATMW
ACQUISITION
CORP.,
MEDSERVE,
INC., and
AVISTA CAPITAL
PARTNERS L.P.,
Defendants.
------------------------------------------------------------------------
Competitive Impact Statement
Plaintiff United States of America (``United States''), pursuant to
Section 2(b) of the Antitrust Procedures and Penalties Act (``APPA'' or
``Tunney Act''), 15 U.S.C. 16(b)-(h), files this Competitive Impact
Statement relating to the proposed Final Judgment submitted for entry
in this civil antitrust proceeding.
I. Nature and Purpose of the Proceeding
Defendant Stericycle, Inc., through ATMW Acquisition Corp., and
defendant MedServe, Inc., through Avista Capital Partners, L.P.,
entered into a stock purchase agreement dated May 9, 2009, pursuant to
which Stericycle would acquire all of the voting shares of MedServe,
valued at $185 million. The United States, and the State of Missouri
and the State of Nebraska (``States''), filed a civil antitrust
Complaint on November 30, 2009, seeking to enjoin the proposed
acquisition. The Complaint alleged that the likely effect of the
acquisition would be to substantially lessen competition in the
provision of infectious waste collection and treatment services for
large quantity generator (``LQG'') customers in the states of Kansas,
Missouri, Nebraska, and Oklahoma, in violation of Section 7 of the
Clayton Act, 15 U.S.C. 18. This loss of competition would result in
higher prices and reduced service for these customers of infectious
waste collection and treatment services.
With the filing of the Complaint in this case, the United States
and the States also filed a Hold Separate Stipulation and Order and
proposed Final Judgment, which are designed to eliminate the
anticompetitive effects of the acquisition. Under the proposed Final
Judgment, explained more fully below, Stericycle and MedServe are
required within ninety (90) days after the filing of the Complaint, or
five (5) days after notice of the entry of the Final Judgment by the
Court, whichever is later, to divest, as a viable business, all of the
MedServe infectious waste collection and treatment assets in Kansas,
Missouri, Nebraska, and Oklahoma. Under the terms of the Hold Separate
Stipulation and Order, Stericycle and MedServe are required to take
certain steps to ensure that the assets to be divested will be
preserved and held separate from their other assets and businesses.
The United States, the States, and the defendants have stipulated
that the proposed Final Judgment may be entered after compliance with
the APPA. Entry of the proposed Final Judgment would terminate this
action, except that the Court would retain jurisdiction to construe,
modify, or enforce the provisions of the proposed Final Judgment and to
punish violations thereof.
II. Description of the Events Giving Rise to the Alleged Violation
A. The Defendants and the Proposed Transaction
Stericycle is a Delaware corporation with its principal place of
business in Lake Forest, Illinois. Stericycle, a multi-national
company, is the largest provider of infectious waste collection and
treatment services in the United States, with operations in nearly all
of the contiguous 48 states, including 46 treatment facilities and 80
transfer and collection sites. In 2008, Stericycle reported total
worldwide sales of approximately $1.1 billion, of which approximately
78 percent were generated in the United States. ATMW Acquisition Corp.
is a corporation formed by Stericycle to facilitate its acquisition of
MedServe.
MedServe is a Delaware corporation with its principal place of
business in Bellaire, Texas. MedServe is the second-largest provider of
infectious waste collection and treatment services in the United
States, with operations in 25 states that include eight treatment
facilities and 18 transfer and collection sites. In 2008, MedServe had
total revenues of about $35 million. Avista Capital Partners, L.P. is
an entity formed by MedServe to facilitate the acquisition of MedServe
by Stericycle.
The proposed transaction, as agreed to by defendants on May 9,
2009, would substantially lessen competition in the provision of
infectious waste collection and treatment services for LQG customers in
the states of Missouri, Nebraska, Oklahoma, and Kansas. This
acquisition is the subject of the Complaint and proposed Final Judgment
filed by the United States and the States on November 30, 2009.
B. The Competitive Effects of the Transaction
1. Relevant Service Market: Infectious Waste Collection and Treatment
Services for LQG Customers
Regulated medical waste is waste generated in the diagnosis,
treatment, or immunization of human beings or animals. There are three
types of regulated medical waste: (1) Infectious waste; (2)
pathological waste; and (3) trace chemotherapy waste. Infectious waste
is waste that comes into contact with bodily fluids and ``sharps''
waste, such as syringes and scalpels. Pathological waste is anatomical
parts, and trace chemotherapy waste is small amounts of chemical
compounds used to treat cancer patients and the equipment used to
administer the compounds. Infectious waste comprises approximately 90
percent of all regulated medical waste generated in the United States.
State and Federal governments heavily regulate the collection and
treatment of regulated medical waste. They prescribe how each type of
regulated medical waste must be stored, collected, and treated.
Providers of infectious waste collection and treatment services are
required to be licensed by the various state and Federal regulatory
agencies before they can offer such services. Regulated medical waste
must be stored separately from other types of waste, and each type of
regulated medical waste must be stored separately from the other types
in specially marked and sealed containers. Collection and transport to
treatment facilities must be performed by a state-approved company.
State-approved treatment facilities must be used to render
regulated medical waste non-infectious. Failure to use state-approved
treatment facilities subjects both the generator of the infectious
waste and the infectious waste collection and treatment service
provider to criminal prosecution, fines, damage actions, and
potentially high clean-up costs.
Autoclaves are the most prevalent treatment technology for
infectious waste. An autoclave uses steam sterilization combined with
pressure to render infectious waste non-infectious. Because autoclaving
is a reliable and long-proven technology for treating infectious waste,
it has become the
[[Page 5129]]
preferred choice for treating infectious waste.
The infectious waste collection and treatment services industry
categorizes customers according to the amount of infectious waste that
they generate. LQG customers typically are hospitals, large
laboratories, and other large medical facilities that generate large
amounts of infectious waste. LQG customers often need collection to
occur on a daily basis, or at least several times a week, and must
receive continuous supplies of containers with sizeable storage
capacity from their service providers.
LQG customers require that their service providers perform both
infectious waste collection and treatment. They also require their
providers to meet strict standards to ensure they have sufficient
technical capability, knowledge, and financial resources. For example,
LQG customers typically require an infectious waste collection and
treatment service provider to have: (a) An adequate infrastructure to
serve the customer's needs, including trucks, storage containers,
transfer stations, electronic equipment capable of monitoring and
tracking each type of waste, and personnel with a variety of expertise
to support the infrastructure; (b) an established reputation for
providing reliable and timely collection and treatment for LQG
customers; (c) its own infectious waste treatment facility to minimize
the number of companies that handle the waste, thereby reducing the
possibility that the waste is mishandled; and (d) substantial liability
insurance that meets all Federal and State regulatory requirements
governing infectious waste.
Collection and treatment service providers bid for each LQG
customer's business separately, and an infectious waste collection and
treatment service provider can identify the specific competitive
conditions that apply to each LQG customer, including which potential
competitors can serve that LQG customer. Infectious waste collection
and treatment service providers for LQG customers can and do price
discriminate based on an LQG customer's requirements and the number of
competitors available to provide such services.
A small but significant increase in the price of infectious waste
collection and treatment services for LQG customers would not cause LQG
customers to move sufficient volumes of infectious waste to another
type of collection and treatment service so as to make such a price
increase unprofitable. Accordingly, the provision of infectious waste
collection and treatment services for LQG customers is a line of
commerce and a relevant price discrimination service market within the
meaning of Section 7 of the Clayton Act.
2. Relevant Geographic Market
The geographic market for the provision of infectious waste
collection and treatment services for LQG customers is largely defined
by transportation costs. Infectious waste collection and treatment
service companies rely on trucks to transport waste from customer sites
to their treatment facilities. Transfer stations enable service
providers to transfer their waste into tractor-trailers and more cost-
effectively transport their waste to treatment facilities. Typically,
the greater the distance between an LQG customer's operations and the
service provider's treatment or transfer facility, the less price
competitive the provider is.
For LQG customers served by MedServe in Kansas, Missouri, Nebraska,
and Oklahoma, the only competitive alternative is Stericycle. In these
states, no other infectious waste collection and treatment service
provider has a facility located within approximately 300 miles of
Stericycle's or MedServe's facilities.
In the states of Kansas, Missouri, Nebraska, and Oklahoma, LQG
customers would not switch to a more distant infectious waste
collection and treatment service provider in sufficient numbers so as
to make a small but significant increase in price unprofitable.
Accordingly, the states of Kansas, Missouri, Nebraska, and Oklahoma are
a relevant geographic market within the meaning of Section 7 of the
Clayton Act.
3. Anticompetitive Effects of the Acquisition
In the states of Kansas, Missouri, Nebraska, and Oklahoma, the
market for the provision of infectious waste collection and treatment
services for LQG customers is highly concentrated. Following the
acquisition, Stericycle would become the monopoly provider of
infectious waste collection and treatment services for LQG customers in
these states.
Vigorous price competition between Stericycle and MedServe in the
provision of infectious waste collection and treatment services has
benefited LQG customers in Kansas, Missouri, Nebraska, and Oklahoma.
Stericycle and MedServe are each other's only rival, directly competing
on price and quality of service in the provision of infectious waste
collection and treatment services for LQG customers.
Therefore, the proposed acquisition will eliminate the competition
between Stericycle and MedServe; reduce the number of providers of
infectious waste collection and treatment services for LQG customers
from two to one; and enable Stericycle to establish a monopoly in the
provision of such services, leading to higher prices and lower quality
of service for LQG customers in Kansas, Missouri, Nebraska, and
Oklahoma, in violation of Section 7 of the Clayton Act.
Successful entry into the provision of infectious waste collection
and treatment services for LQG customers in Kansas, Missouri, Nebraska,
and Oklahoma would be difficult, time-consuming, and costly. A
prospective provider of infectious waste collection and treatment
services for LQG customers faces substantial financial and permitting
requirements to build a facility and the infrastructure needed to serve
LQG customers. It also must have an established reputation for handling
large amounts of infectious waste produced by LQG customers. A provider
of infectious waste collection and treatment services for LQG customers
in Kansas, Missouri, Nebraska, and Oklahoma must establish a treatment
facility that contains a treatment technology, such as an autoclave,
with sufficient capacity for treating large volumes of infectious
waste. In addition to the capital costs of the treatment unit, local
zoning and state permits are required.
A provider of infectious waste collection and treatment services
for LQG customers also must have an infrastructure of trucks, transfer
stations, and electronic equipment capable of collecting, transporting,
treating and disposing, and monitoring and tracking the infectious
waste.