2026 – Federal Register Recent Federal Regulation Documents
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Medicare Program; CY 2027 Changes to the End-Stage Renal Disease (ESRD) Prospective Payment System, Acute Kidney Injury Dialysis (AKI) Payment, and ESRD Quality Incentive Program
This proposed rule would update and revise the End-Stage Renal Disease (ESRD) Prospective Payment System for calendar year 2027. This rule also proposes to update the payment rate for renal dialysis services furnished by an ESRD facility to individuals with acute kidney injury. In addition, this rule proposes to update the requirements for the ESRD Quality Incentive Program.
Nondiscrimination in Federally-Assisted Programs of the Department of Veterans Affairs
The Department of Veterans Affairs (VA) proposes to amend its regulations implementing Title VI of the Civil Rights Act of 1964 (Title VI) to eliminate disparate-impact liability. These amendments would align VA's regulations with Title VI's original public meaning, avoid constitutional concerns, reduce compliance costs, serve the public interest, and implement changes directed in Executive Order (E.O.) 14281. This is a deregulatory action in furtherance of E.O. 14219, which requires that Federal regulations reflect the best reading of the underlying statutory authority.
Transport Airplane and Propulsion Certification Modernization
FAA proposes to amend various airworthiness regulations to modernize certain certification standards for transport category airplanes and propulsion systems. This rule would be both deregulatory and relieving by reducing the number of exemptions, special conditions, and equivalent level of safety findings required during the certification process. FAA expects that this proposal would reduce certification costs and time to certify new and changed products for both industry and FAA while maintaining or increasing the level of safety provided by the current regulations. FAA proposes to remove Special Federal Aviation Regulation (SFAR) No. 109 from part 25 and relocate certain of its requirements. Finally, this action would address industry and National Transportation Safety Board recommendations while also harmonizing FAA's regulations with international standards.
Air Plan Approval; Ohio; Source-Specific Non-CTG RACT and SIP Strengthening for Ohio
The Environmental Protection Agency (EPA) is approving source- specific State Implementation Plan (SIP) revisions submitted by Ohio. These revisions address major source volatile organic compound (VOC) and nitrogen oxide (NOX) reasonably available control technology (RACT) requirements for the Cleveland, OH Moderate nonattainment area for the 2015 ozone National Ambient Air Quality Standard (NAAQS or standard). The affected facilities include PPG Industries Ohio, Inc. (PPG), Owens Corning, Akron Paint and Varnish, Charter Steel, U. S. Steel Tubular Lorain, Carmeuse Lime, and Ross Incineration. The EPA is also approving source-specific SIP revisions for General Electric Aviation Evendale and Tyson Foods for the Cincinnati maintenance area for the 2015 ozone standard. Finally, the EPA is rescinding the source-specific VOC RACT rule for Formica Corporation since it is subject to an equivalent CTG-based rule in the Ohio Administrative Code (OAC). The EPA proposed to approve this action on February 27, 2026, and received five comments.
Air Plan Approval; Ohio; Source-Specific Non-CTG RACT
The Environmental Protection Agency (EPA) is approving source- specific State Implementation Plan (SIP) revisions submitted by Ohio. These revisions address major source volatile organic compound (VOC) and nitrogen oxide (NOX) reasonably available control technology (RACT) requirements for the Cleveland, OH Moderate nonattainment area (Cuyahoga, Geauga, Lake, Lorain, Medina, Portage, and Summit counties) for the 2015 ozone National Ambient Air Quality Standard (NAAQS or standard). The affected facilities include Lubrizol, Henkel, and Cleveland-Cliffs Cleveland Works. With this approval, Ohio has fully satisfied the Moderate area RACT requirements of the Clean Air Act (CAA) with respect to the 2015 ozone standard for the Cleveland area.
Bus Testing: Updates to Bus Testing Program Procedures and Policies, Clarifications, Technical Adjustments, and Other Program Updates
The Federal Transit Administration (FTA) is proposing amendments to its bus testing regulation. The proposed changes will improve the efficiency of the testing program for stakeholders, enhance the value of bus testing reports for consumers, and assist in removing outdated test reports.
Agency Information Collection Activities; Notice and Request for Comment; 49 CFR Part 569, 571.110, 571.120 & 574, Compliance and Labeling of Motor Vehicle Tires and Rims
The National Highway Traffic Safety Administration (NHTSA) invites public comments about our intention to request approval from the Office of Management and Budget (OMB) for reinstatement with change of a previously approved information collection. Before a Federal agency can collect certain information from the public, it must receive approval from OMB. Under procedures established by the Paperwork Reduction Act of 1995, before seeking OMB approval, Federal agencies must solicit public comment on proposed collections of information, including extensions and reinstatements of previously approved collections. This document describes a collection of information for which NHTSA intends to seek OMB approval and solicits public comments on continuation of the requirements on tire identification and recordkeeping and the accuracy of the agency's revised estimates of the burden of the information collections. The cost estimate for this reinstatement has increased by $37,000, from $970,620 to $1,007,620. This rise is primarily due to an estimated increase in the number of vehicles from 19,000,000 to 20,000,000, which has raised the number of rims from 95,000,000 to 100,000,000. As a result, the total annual costs for recordkeepers associated with rims have grown from $703,000 to $740,000. The higher vehicle estimate also increases the annual burden for information collection by new tire manufacturers, retreaders, and rim manufacturers to 278,913 hours, up from 274,491 hours in the previous request.
Commission Information Collection Activities (Ferc-725b). Comment Request; Errata Notice
In compliance with the requirements of the Paperwork Reduction Act of 1995, the Federal Energy Regulatory Commission (Commission or FERC) is soliciting public comment on the currently approved information collection, FERC-725B, (Mandatory Reliability Standards, Critical Infrastructure Protection (CIP)). This submission is for an extension request and changes to CIP-002-8. No comments were received on the 60-day notice. This notice corrects the 30-day notice published on June 12, 2026 (91 FR 35681) adjusting the estimates in the burden table.
Removing Obsolete References to Twentieth-Century Airman Certificates
FAA proposes to remove obsolete references to pilot certificates and ratings issued more than 50 years ago.
Modernizing Security Requirements
The U.S. Nuclear Regulatory Commission (NRC) is proposing to revise its regulations to modernize security and fitness-for-duty requirements to enhance efficiency, consistent with Executive Order 14300, "Ordering the Reform of the Nuclear Regulatory Commission." The proposed revisions are intended to reduce regulatory burden, where appropriate, while continuing to provide reasonable assurance that safety and security will be adequately maintained at NRC-licensed facilities.
Notice of Determinations; Culturally Significant Object Being Imported for Exhibition-Determinations: “Georgia O'Keeffe Architecture” Exhibition
Notice is hereby given of the following determinations: I hereby determine that a certain object being imported from abroad pursuant to an agreement with its foreign owner or custodian for temporary display in the exhibition "Georgia O'Keeffe Architecture" at the Detroit Institute of Arts, Detroit, Michigan, and at possible additional exhibitions or venues yet to be determined, is of cultural significance, and, further, that its temporary exhibition or display within the United States as aforementioned is in the national interest. I have ordered that Public Notice of these determinations be published in the Federal Register.
Federal Motor Vehicle Safety Standards; Modernization of FMVSS No. 135 To Accommodate ADS-Equipped Vehicles
NHTSA is proposing to amend Federal Motor Vehicle Safety Standard (FMVSS) No. 135, "Light vehicle brake systems." The proposed modifications would distinguish how regulations apply to vehicles with and without manually operated driving controls. The proposed modifications would clarify definitions, telltale requirements, performance requirements, and test procedures in the standard and remove sections that are no longer relevant. The stopping distance performance requirements, which address the primary safety purpose of the standard, would still apply to all subject vehicles. This rulemaking would remove unnecessary regulatory burdens and costs without detriment to vehicle safety.
ADS-Equipped Vehicle Safety, Transparency, and Evaluation Program; Withdrawal
This action withdraws the notice of proposed rulemaking (NPRM) published in the Federal Register on January 15, 2025, which proposed to establish the Automated Driving System-Equipped Vehicle Safety, Transparency, and Evaluation Program (AV STEP). The proposal would have created a voluntary program for vehicle manufacturers, developers of Automated Driving Systems (ADS), and fleet operators or system integrators of such vehicles. Based on its reevaluation of the proposal, consideration of the comments received, and subsequent progress on other ADS initiatives, NHTSA is withdrawing the rulemaking.
Agency Information Collection Activities: Request for Comments for a New Information Collection
The FHWA has forwarded the information collection request described in this notice to the Office of Management and Budget (OMB) to approve a new information collection. We are required to publish this notice in the Federal Register by the Paperwork Reduction Act of 1995.
Meeting of the Regional Energy Resource Council
The TVA Regional Energy Resource Council (RERC) will hold a meeting on July 14, 2026, to receive an update and provide advice on TVA's 2026 Integrated Resource Plan (IRP). The IRP provides strategic direction on how TVA will continue to provide low-cost, reliable, and resilient electricity to the 10 million residents of the Valley region.
List of Bulk Drug Substances for Which There Is a Clinical Need Under Section 503B of the Federal Food, Drug, and Cosmetic Act; Extension of Comment Period
The Food and Drug Administration (FDA or the Agency) is extending the comment period for the notice entitled "List of Bulk Drug Substances for Which There Is a Clinical Need Under Section 503B of the Federal Food, Drug, and Cosmetic Act" that appeared in the Federal Register of May 1, 2026. In the Federal Register notice, FDA requested comments on FDA's proposal not to include semaglutide, tirzepatide, or liraglutide on a list of bulk drug substances (active pharmaceutical ingredients) for which there is a clinical need for outsourcing facilities to use in compounding (the 503B Bulks List). The Agency is taking this action in response to a request for an extension to allow interested persons additional time to submit comments.
Air Quality Plan; California; Mojave Desert Air Quality Management District; Rescissions of Outdated Requirements Within Riverside County
The Environmental Protection Agency (EPA) is proposing to approve revisions to the Mojave Desert Air Quality Management District (MDAQMD or "District") portion of the California State Implementation Plan (SIP). These revisions concern prohibitory rules that regulate emissions of volatile organic compounds (VOCs) and oxides of nitrogen (NOX) under the Clean Air Act (CAA or "Act") within the Riverside County portion of the MDAQMD portion of the California SIP. We are proposing to approve the rescissions of the rules because the requirements in the rules are no longer necessary to retain in the SIP to meet CAA requirements.
Drugs for Human Use; Drug Efficacy Study Implementation: Estrogen-Androgen Fixed-Combination Drug Products; Extension of Effective Date of Final Resolution of Drug Efficacy Study Implementation 7661
The Food and Drug Administration (FDA, Agency, or we) is extending the effective date of the notice published in the Federal Register on May 27, 2026, titled Drugs for Human Use; Drug Efficacy Study Implementation: Estrogen-Androgen Fixed-Combination Drug Products; Syntest D.S. and Syntest H.S. Tablets; Withdrawal of Hearing Requests; Final Resolution of Drug Efficacy Study Implementation 7661 (91 FR. 31462) (the "May 2026 Notice"), by 90 days. The effective date of the May 2026 Notice is hereby extended from June 26, 2026, to September 24, 2026. This extension is necessary to allow FDA sufficient time to consider issues raised by interested parties following publication of the May 2026 Notice.
Southern California Annual Firework Events for the Los Angeles Long Beach Captain of the Port Zone
The Coast Guard will enforce safety zones for annually reoccurring fireworks events taking place on July 4, 2026 in the Los AngelesLong Beach Captain of the Port Zone. This action is necessary and intended to provide for the safety of life and property on the navigable waterways during these events. During the enforcement periods, the operator of any vessel in the regulated area must comply with directions from the Patrol Commander or any official patrol vessel.
Agency Information Collection Activities; Proposed Information Collection Request; Comment Request; Emergency Planning and Community Right to Know Act (EPCRA) and Comprehensive Environmental Response, Compensation, and Liability Act (CERCLA) Continuous Release Reports
The Environmental Protection Agency (EPA) is planning to submit an information collection request (ICR), "Emergency Planning and Community Right to Know Act (EPCRA) and Comprehensive Environmental Response, Compensation, and Liability Act (CERCLA) Continuous Release Reports" (EPA ICR Number 1445.16, OMB Control Number 2050-0086) to the Office of Management and Budget (OMB) for review and approval in accordance with the Paperwork Reduction Act (PRA). Before doing so, EPA is soliciting public comments on specific aspects of the proposed information collection as described below. This is a proposed extension of the ICR, which is currently approved through April 30, 2027. This document allows for 60 days for public comments.
Agency Information Collection Activities; Proposed Information Collection Request; Comment Request; Emergency Planning and Community Right-to-Know Act (EPCRA) Emergency Notifications
The Environmental Protection Agency (EPA) is planning to submit an information collection request (ICR), "Emergency Planning and Community Right-to-Know Act (EPCRA) Emergency Notifications" (EPA ICR Number 1395.11, OMB Control Number 2050-0092) to the Office of Management and Budget (OMB) for review and approval in accordance with the Paperwork Reduction Act (PRA). Before doing so, EPA is soliciting public comments on specific aspects of the proposed information collection as described below. This is a proposed extension of the ICR, which is currently approved through March 31, 2027. This document allows for 60 days for public comments.
Takes of Marine Mammals Incidental to Specified Activities; Taking Marine Mammals Incidental to the U.S. Army Corps of Engineers Bonneville Lock 1 Bridge Replacement Project on the Columbia River in Oregon.
NMFS has received a request from U.S. Army Corps of Engineers (USACE) for authorization to take marine mammals incidental to 2 years of construction activities associated with the Bonneville Lock 1 Bridge Replacement (BLBR) Project on the Columbia River in Oregon. Pursuant to the Marine Mammal Protection Act (MMPA), NMFS is requesting comments on its proposal to issue two consecutive incidental harassment authorizations (IHAs) to incidentally take marine mammals during the specified activities. NMFS is also requesting comments on possible one- time, 1-year renewals that could be issued under certain circumstances and if all requirements are met, as described in Request for Public Comments at the end of this notice. NMFS will consider public comments prior to making any final decision on the issuance of the requested MMPA authorizations.
U.S. Ecology Nevada, Inc. High Mercury Subcategory Wastes Land Disposal Restrictions Variance
The Environmental Protection Agency (EPA) is granting, with conditions, U.S. Ecology Nevada Inc.'s (USE) petition for a site- specific treatability variance (SSTV) from the Resource Conservation and Recovery Act (RCRA) Land Disposal Restrictions (LDR) treatment standards. USE's petition is for a variance from the existing treatment and disposal standard for elemental mercury waste generated from retorting high mercury waste as prescribed by the LDR technology-based standard of RMERC. The petition demonstrated that the LDR standard for placing elemental mercury waste generated from RMERC back into commerce for reuse is inappropriate and the alternative treatment variance proposed by USE is sufficient to minimize threats to human health and the environment posed by land disposal of the waste. Under the approved SSTV, the existing LDR treatment standard of RMERC will continue to apply to high mercury hazardous wastes, but the elemental mercury generated from this process will be treated and land disposed subject to specified conditions at both Bethlehem Apparatus's facility in Bethlehem, Pennsylvania, and USE's Beatty, Nevada, subtitle C treatment, storage, and disposal (TSD) facility where the treated mercury wastes will be disposed in a designated RCRA subtitle C compliant monofill.
Medical Devices; Neurological Devices; Classification of the External Lower Extremity Nerve Stimulator for Restless Legs Syndrome
The Food and Drug Administration (FDA) is classifying the external lower extremity nerve stimulator for Restless Legs Syndrome into class II (special controls). The special controls that apply to the device type are identified in this order and will be part of the codified language for classification of the external lower extremity nerve stimulator for Restless Legs Syndrome. We are taking this action because we have determined that classifying the device into class II will provide a reasonable assurance of safety and effectiveness of the device. We believe this action will also enhance patients' access to beneficial innovative devices, in part by reducing regulatory burdens.
Medical Devices; General and Plastic Surgery Devices; Classification of the Breast Implant Suction Retrieval System
The Food and Drug Administration (FDA) is classifying the breast implant suction retrieval system into class II (special controls). The special controls that apply to the device type are identified in this order and will be part of the codified language for classification of the breast implant suction retrieval system. We are taking this action because we have determined that classifying the device into class II will provide a reasonable assurance of safety and effectiveness of the device. We believe this action will also enhance patients' access to beneficial innovative devices, in part by reducing regulatory burdens.
Medical Devices; Immunology and Microbiology Devices; Classification of the SARS-CoV-2 Serology Test
The Food and Drug Administration (FDA) is classifying the SARS-CoV-2 serology test into class II (special controls). The special controls that apply to the device type are identified in this order and will be part of the codified language for classification of the SARS- CoV-2 serology test. We are taking this action because we have determined that classifying the device into class II will provide a reasonable assurance of safety and effectiveness of the device. We believe this action will also enhance patients' access to beneficial innovative devices, in part by reducing regulatory burdens.
Medical Devices; Neurological Devices; Classification of the Computerized Behavioral Therapy Device for the Treatment of Fibromyalgia Symptoms
The Food and Drug Administration (FDA) is classifying the computerized behavioral therapy device for the treatment of fibromyalgia symptoms into class II (special controls). The special controls that apply to the device type are identified in this order and will be part of the codified language for classification of the computerized behavioral therapy device for the treatment of fibromyalgia symptoms. We are taking this action because we have determined that classifying the device into class II will provide a reasonable assurance of safety and effectiveness of the device. We believe this action will also enhance patients' access to beneficial innovative devices, in part by reducing regulatory burdens.
Medical Devices; Clinical Chemistry and Toxicology Devices; Classification of the Prognostic Test for Development or Progression of Preeclampsia
The Food and Drug Administration (FDA) is classifying the prognostic test for development or progression of preeclampsia into class II (special controls). The special controls that apply to the device type are identified in this order and will be part of the codified language for classification of the prognostic test for development or progression of preeclampsia. We are taking this action because we have determined that classifying the device into class II will provide a reasonable assurance of safety and effectiveness of the device. We believe this action will also enhance patients' access to beneficial innovative devices, in part by reducing regulatory burdens.
Medical Devices; General Hospital and Personal Use Devices; Classification of the Foam or Gel Chemical Sterilant/High Level Disinfectant
The Food and Drug Administration (FDA) is classifying the foam or gel chemical sterilant/high level disinfectant into class II (special controls). The special controls that apply to the device type are identified in this order and will be part of the codified language for classification of the foam or gel chemical sterilant/high level disinfectant. We are taking this action because we have determined that classifying the device into class II will provide a reasonable assurance of safety and effectiveness of the device. We believe this action will also enhance patients' access to beneficial innovative devices, in part by reducing regulatory burdens.
Air Plan Approval; District of Columbia; Creation of Synthetic Minor Permit Program
The Environmental Protection Agency (EPA) is approving a state implementation plan (SIP) revision submitted by the Department of Energy and Environment (DOEE) on behalf of the District of Columbia (DC). The revision pertains to creating a synthetic minor permit program and resolving the regulatory differences between DC's current regulations and those regulations approved previously in Chapters 1 and 2 of the Air Quality Regulations codified in title 20 of the District of Columbia Municipal Regulations (DCMR). The intended effect of this action is to enable DC to create federally enforceable synthetic minor permit conditions for sources of criteria pollutants. The EPA is approving these revisions to the DC SIP in accordance with the requirements of the Clean Air Act (CAA).
Safety Zone; Ohio River MM 602.0-605.0, Louisville, KY
The Coast Guard is establishing a temporary safety zone for navigable waters on the Ohio River from MM 602.0-605.0. The safety zone is needed to protect personnel, vessels, and the marine environment from potential hazards associated with an over water fireworks display. Entry of vessels or persons into this zone is prohibited unless specifically authorized by the Captain of the Port, Ohio Valley, or their designated representative.
Approval and Promulgation of State Air Quality Plans for Designated Facilities and Pollutants; Oklahoma; Control of Emissions From Existing Other Solid Waste Incineration Units, Hospital/Medical/Infectious Waste Incinerator Units, and Commercial and Industrial Solid Waste Incineration Units
Pursuant to the Federal Clean Air Act (CAA or the Act), the Environmental Protection Agency (EPA) is notifying the public that we have received CAA section 111(d)/129 negative declarations from Oklahoma for existing incinerators subject to the Other Solid Waste Incineration units (OSWI), Hospital/Medical/Infectious Waste Incinerator units (HMIWI), and Commercial and Industrial Solid Waste Incineration Units (CISWI) Emission Guidelines (EG). These negative declarations certify that existing incinerators subject to the OSWI, HMIWI, and CISWI EG and the requirements of sections 111(d) and 129 of the CAA do not exist within specified jurisdictions in Oklahoma. The EPA is accepting these negative declarations and amending agency regulations in accordance with the requirements of the CAA.
Approval and Promulgation of State Air Quality Plans for Designated Facilities and Pollutants; Louisiana; Control of Emissions From Existing Other Solid Waste Incineration Units
Pursuant to the Federal Clean Air Act (CAA or the Act), the Environmental Protection Agency (EPA) is notifying the public that we have received a CAA section 111(d)/129 negative declaration from Louisiana for existing incinerators subject to the Other Solid Waste Incineration units (OSWI) Emission Guidelines (EG). This negative declaration certifies that existing incinerators subject to the OSWI EG and the requirements of sections 111(d) and 129 of the CAA do not exist within specified jurisdictions in Louisiana. The EPA is accepting the negative declaration and amending the agency regulations in accordance with the requirements of the CAA.
Notice of OFAC Sanctions Action
The U.S. Department of the Treasury's Office of Foreign Assets Control (OFAC) is publishing the name of one or more persons that have been placed on OFAC's Specially Designated Nationals and Blocked Persons List (SDN List) based on OFAC's determination that one or more applicable legal criteria were satisfied. All property and interests in property subject to U.S. jurisdiction of these persons are blocked, and U.S. persons are generally prohibited from engaging in transactions with them. Additionally, OFAC is publishing updates to the identifying information of one person currently included on the SDN List.
Agency Information Collection Activities; Notice and Request for Comments; Names and Addresses of First Purchasers of Motor Vehicles and Tire Identification and Recordkeeping Requirements
The National Highway Traffic Safety Administration (NHTSA) invites public comments about our intention to request approval from the Office of Management and Budget (OMB) for a reinstatement of a previously approved information collection. Before a Federal agency can collect certain information from the public, it must receive approval from OMB. Under procedures established by the Paperwork Reduction Act of 1995, before seeking OMB approval, Federal agencies must solicit public comment on proposed collections of information, including extensions and reinstatements of previously approved collections. This document describes a collection of information for which NHTSA intends to seek OMB approval and solicits public comments on continuation of the requirements on tire identification and recordkeeping and the accuracy of the agency's revised estimates of the burden of the information collections.
New Postal Products
The Commission is noticing a recent Postal Service filing for the Commission's consideration concerning a negotiated service agreement. This notice informs the public of the filing, invites public comment, and takes other administrative steps.
Cinnamaldehyde in Pesticide Formulations; Exemption From the Requirement for a Tolerance
This regulation establishes an exemption from the requirement of a tolerance for residues of cinnamaldehyde (CAS Reg. No. 104-55-2) when used as an inert ingredient (preservative/stabilizer) on growing crops and raw agricultural commodities pre- and post-harvest, limited to no more than 100 parts per million (ppm) in the end-use pesticide formulation. Wagner Regulatory Associates, Inc., on behalf of Minagro, submitted a petition to EPA under the Federal Food, Drug, and Cosmetic Act (FFDCA), requesting establishment of an exemption from the requirement of a tolerance. This regulation eliminates the need to establish a maximum permissible level for residues of cinnamaldehyde, when used in accordance with the terms of this exemption.
Response to Petition for Reconsideration, Federal Motor Vehicle Safety Standards; Seat Belt Assembly Anchorages
NHTSA published a final rule on September 17, 2024 that amended the regulation on seat belt assembly anchorages. The final rule updated the test procedure for existing test devices and added an alternative test device as a compliance option. In response to the 2024 final rule, the agency received a petition for reconsideration from the Truck and Engine Manufacturers Association. After considering the petition, NHTSA is proposing to delay the compliance date from September 1, 2027 to September 1, 2030 for vehicles with a Gross Vehicle Weight Rating (GVWR) of greater than 4,536 kg.
Notice of Extended Modification to the Special Use Permit (SUP) Category for the Continued Presence of Commercial Submarine Cables Within the National Marine Sanctuary System
NOAA hereby provides public notice that it is extending the temporary suspension of the special use permit (SUP) category for the continued presence of commercial submarine cables on or within national marine sanctuaries so that, for an additional two-year period until August 16, 2028, the SUP category does not apply to commercial submarine cables in sanctuaries designated after August 16, 2024. NOAA is continuing to evaluate options for permitting submarine cables in sanctuaries, including through a separate rulemaking action.
Rio Grande LNG Train 6, LLC; Application for Long-Term Authorization To Export Liquefied Natural Gas to Non-Free Trade Agreement Nations
The Hydrocarbons and Geothermal Energy Office (HGEO) of the Department of Energy (DOE) gives notice (Notice) of receipt of an application (Application), filed by Rio Grande LNG Train 6, LLC (RGLNG Train 6) on June 11, 2026. RGLNG Train 6 requests long-term, multi- contract authorization to export domestically produced liquefied natural gas (LNG) in a volume equivalent to approximately 312.05 billion cubic feet (Bcf) of natural gas per year (Bcf/yr) from the proposed Rio Grande LNG Expansion Project (Project), to be located at and adjacent to the previously authorized Rio Grande LNG Terminal (RGLNG Terminal), along the Brownsville Ship Channel in Cameron County, Texas. RGLNG Train 6 filed the Application under the Natural Gas Act (NGA).
Evaluation of the California Coastal Management Program; Notice of Public Meetings; Request for Comments
The National Oceanic and Atmospheric Administration (NOAA)'s Office for Coastal Management will hold both an in-person meeting and two virtual public meetings to solicit input for a performance evaluation of the California Coastal Management Program. These meetings are intended to provide the public with the opportunity to add to the input obtained from the previous public meeting held in August 2024. In particular, NOAA seeks any new input from relevant stakeholders regarding spaceport infrastructure, offshore oil production, pipeline maintenance, desalination projects, and undersea cables.
Revocation of Three Authorizations of Emergency Use of In Vitro Diagnostic Devices for Detection and/or Diagnosis of COVID-19; Availability
The Food and Drug Administration (FDA) is announcing the revocation of the Emergency Use Authorizations (EUAs) (the Authorizations) issued to Becton, Dickinson and Company (BD) for the BD Veritor System for Rapid Detection of SARS-CoV-2, InBios International, Inc. for the SCoV-2 Detect Neutralizing Ab ELISA, and Roche Diagnostics for the Elecsys Anti-SARS-CoV-2. FDA revoked the Authorizations under the Federal Food, Drug, and Cosmetic Act (FD&C Act) as requested by the Authorization holder. The revocations, which include an explanation of the reasons for each revocation, are reprinted at the end of this document.
Medical Devices; General Hospital and Personal Use Devices; Classification of the Infant Supine Sleep System
The Food and Drug Administration (FDA) is classifying the infant supine sleep system into class II (special controls). The special controls that apply to the device type are identified in this order and will be part of the codified language for classification of the infant supine sleep system. We are taking this action because we have determined that classifying the device into class II will provide a reasonable assurance of safety and effectiveness of the device. We believe this action will also enhance patients' access to beneficial innovative devices, in part by reducing regulatory burdens.
