Compilation of Rules and Regulations of the State of Georgia
Department 351 - GEORGIA ACCESS TO MEDICAL CANNABIS COMMISSION
Chapter 351-6 - DISPENSING LICENSEES
Rule 351-6-.09 - Recall Procedures
Universal Citation: GA Rules and Regs r 351-6-.09
Current through Rules and Regulations filed through December 18, 2024
(1) A dispensing licensee shall establish, maintain, and follow standard operating procedures for licensee-initiated or Commission-ordered recalls of product in final packaged form. Such procedures shall address, at a minimum, the following:
(a) Notifications to patients, caregivers, and the public;
(b) Reporting adverse events and symptoms experienced by patients to the originating production licensee and the Commission and its employees;
(c) The collection of such recalled product;
(d) The quarantine and storage of such recalled product that have not been dispensed;
(e) The quarantine and storage of such recalled product that would be returned; and
(f) The return of such recalled product to the originating production licensee.
(2) The dispensing licensee shall display a public notice of a licensee-initiated or Commission-ordered recall until the termination of the recall. Such notice shall be:
(a) Received from the originating production licensee responsible for the recall;
(b) Posted within twenty-four (24) hours of the recall being initiated;
(c) Displayed in a conspicuous location, unobstructed, and easily viewable for patients and caregivers; and
(d) Posted in a prominent location of the dispensing licensee's website and social media, if the dispensary impacted by the recall has a website separate from the originating production licensee.
(3) Upon receipt of a written notice for a recall, a dispensing licensee shall ensure product in final packaged form subject to the recall is:
(a) Removed from availability for retail purchase or transfer; and
(b) Quarantined and stored from all other product in final packaged form that is not part of the recall.
O.C.G.A. §§ 16-12-203, 16-12-206, 16-12-210.
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