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US (MI): BMR adds two prodcuts to Detroit marijuana product recall

The Dept. of Licensing and Regulatory Affairs (LARA) issued an updated health and safety advisory due to the sale of marijuana which failed laboratory testing. Two additional products – Purple Sherbet #2 and Do Si Do – were added to the original recall of four products from the Green Mile Detroit on January 10, 2019.

All marijuana product subject to recall in this notice was purchased by the licensed facility from a registered primary caregiver under a resolution by the Medical Marihuana Licensing Board passed on January 16, 2019.

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

This recall affects the following marijuana products sold from The Green Mile Detroit – License PC-000144 – located at 6650 E Eight Mile RD Detroit, MI 48234:

Updated recalled products (2/7/19):
Purple Sherbet #2 (flower)
1A405010000076E000000155
Failed for chemical residue

Do Si Do (flower)
1A405010000076E000000151
Failed for chemical residue

Patients or caregivers who have these affected medical marijuana products in their possession should return them to The Green Mile Detroit for proper disposal.  The Green Mile Detroit must notify patients or caregivers that purchased these medical marijuana products of the recall.

Updated Public Health and Safety Advisory Bulletins
In addition to the products updated for the Green Mile Detroit recall, BMR also updated multiple Public Health and Safety Advisory Bulletins, adding the following sentence to each bulletin:

All marijuana product subject to recall in this notice was purchased by the licensed facility from a registered primary caregiver under a resolution by the Medical Marihuana Licensing Board passed on January 16, 2019.

Source: michigan.gov

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