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Michigan Issues First Recall Of Marijuana Products

Michigan has issued its first recall on marijuana products after the state began regulating medical marijuana last year, saying that the products supplied to provisioning centers were not laboratory-tested.

The Department of Licensing and Regulatory Affairs or LARA said Friday that it has issued a health and safety advisory due to the release of non-laboratory tested marijuana products supplied to provisioning centers by Jackson, Michigan-based Choice Labs, LLC.

LARA noted that Choice Labs and the Bureau of Marijuana Regulation are taking precautionary steps to issue the voluntary recall as marijuana patients may be immunocomprised.

Patients or caregivers who have these affected medical marijuana products in their possession should return them to the provisioning center from which they were purchased for proper disposal or retesting, according to LARA.

The department also urged provisioning centers to notify patients or caregivers who have purchased these medical marijuana products of the recall.

Choice Labs will dispose of or retest the recalled medical marijuana products.

All affected medical marijuana has a label affixed to the container that, at a minimum, indicates the license number of the marijuana facility that manufactured the marijuana product, as well as the production batch number assigned to the marijuana product.

This recall affects the following batches under Processor License PR-000005:
1A4050100000900000000035, 1A4050100000900000000046, 1A4050100000900000000064, 1A4050100000900000000073, 1A4050100000900000000075, 1A4050100000900000000077, 1A4050100000900000000138, 1A4050100000900000000164 and 1A4050100000900000000167.

Only the products with the above batch numbers are being recalled.

Products affected bv the recall include Mary's Transdermal Indica Patches, The Remedy Tincture-Mary's, Mary's Transdermal Patches CBD, The Coltyn 1:1 Tincture, and Mary's Transdermal 1:1 Patches.

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