New Mexico Administrative Code
Title 7 - HEALTH
Chapter 34 - MEDICAL USE OF CANNABIS
Part 4 - LICENSING REQUIREMENTS FOR PRODUCERS, PRODUCTION FACILITIES AND DISTRIBUTION
Section 7.34.4.24 - RECALLS OF USABLE CANNABIS

Universal Citation: 7 NM Admin Code 7.34.4.24

Current through Register Vol. 35, No. 18, September 24, 2024

A. All non-profit producers and approved manufacturers shall establish and implement written procedures for recalling usable cannabis and products that have been sold or otherwise distributed to qualified patients, primary caregivers, or other cannabis establishments. Recall procedures shall be made available for the department's inspection upon request. The recall procedures shall identify:

(1) The circumstances in which a recall will be conducted, including but not limited to circumstances involving the mislabeling of products and the contamination of products.

(2) Personnel responsible for implementing the recall procedures.

(3) Procedures for notification of all customers who have, or reasonably could have, obtained an affected product, including communication and outreach via media, as appropriate.

(4) Procedures for notification of any other cannabis establishment that supplied or received the recalled product.

(5) Instructions to be provided to qualified patients, primary caregivers, and cannabis establishments for the return or destruction of the recalled product.

(6) Procedures for the collection and wastage (as may be required by this rule) of any recalled product, which shall meet the requirements of this section.

B. All recalled products that are intended to be destroyed shall be wasted in accordance with the wastage requirements of this rule.

C. The licensee shall notify the department of any recall within 24 hours of initiating the recall.

D. The department may order the immediate recall of a usable cannabis product if it deems such action necessary to protect public health and safety.

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