Recall

Michigan Recalls Cannabis Products Sold from 11/22 to 01/22 Due to Chemical and Arsenic Residue

The Michigan Department of Licensing and Regulatory Affairs (LARA) issued a health and safety advisory recall of thirteen (13) cannabis product sold at Kenzy Consulting, Inc. (The Patient Station) between 11/14/2018 and 01/22/2019. LARA has required Kenzy Consulting to inform qualifying patients of the recall. The recalled cannabis products failed several tests including moisture content, chemical and arsenic residue.

Michigan Recalls Cannabis Sold Between December 4th and January 3rd: 5th Recall in January

The Michigan Department of Licensing and Regulatory Affairs (LARA) issued a public health and safety advisory recall of marijuana products sold at Indica, LLC between 12/04/2018 and 01/03/2019. The recalled cannabis products including Black Cherry Pie Buds, Punch Shatter, Gorilla Dosha Buds, Shatter, Galactic Meds Polar Bar, and Purple Kush failed a wide range of tests including yeast, mold, and chemical residue. LARA has required Indica, LLC to inform qualifying patients of the recall.

Michigan Cannabis Business Recalls Untested Products

The Michigan Department of Licensing and Regulatory Affairs issued a Health and Safety Advisory informing consumers that cannabis business, Choice Labs LLC, issued a voluntary recall of untested cannabis products. The contaminated cannabis includes 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. Consumers are instructed to return the products to the store where they were purchased.