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Medical marijuana recall notice

Mary Drier

Mon, 13 Jan 2020 15:28:01 EST

 


click on the picture to enlarge







The Marijuana Regulatory Agency (MRA) issued a health and safety advisory bulletin regarding the recall of medical marijuana product 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.

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 who purchased these medical marijuana products of the recall.

This recall affects the following products sold at three provisioning centers in the state of Michigan between 10/14/2019 and 1/6/2020:

Production batch: 1A4050100002330000000009
Product name: Orange Burst - Buds
Failed testing: Chemical Residue (Paclobutrazol)

Pharmaco, Inc. (License # PC-000249)
3650 Patterson RD
Bay City MI 48706
Individual Package # 1A4050100002330000000415

Pharmaco, Inc. (License # PC-000261)
3557 Wilder RD
Bay City MI 48706
Individual Package # 1A4050100002330000000416   

Pharmaco, Inc. (License # PC-000205)
20561 Dwyer ST
Detroit MI 48234
Individual Package # 1A405010000233000000041


   

 

 

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