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Marijuana Regulatory Agency Expands Product Recall
USAgNet - 01/20/2020

The Marijuana Regulatory Agency (MRA) issued a health and safety advisory bulletin on Friday due to the recall of medical marijuana products which failed safety compliance testing.

All affected medical marijuana is required to have a label affixed to the container that indicates the METRC number assigned to the marijuana product. Patients and caregivers should look for the production batch number associated with the product name or the individual package number which can be found under the name of the provisioning center at which the product was sold.

Recalled products are listed at https://bit.ly/2RxXDW4.

Patients or caregivers who have these affected medical marijuana products in their possession should return them to the provisioning center where they were purchased for proper disposal. Provisioning centers who carried the products must notify patients or caregivers that purchased these medical marijuana products of the recall.

Patients and caregivers are requested to report any adverse product reactions to the MRA via email: MRA-Enforcement@michigan.gov or via phone: 517-284-8597.

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