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Marijuana Products Recalled in Lansing
Media Contact: LARA Communications 517-373-9280
January 11, 2019 – The Dept. of Licensing and Regulatory Affairs (LARA) issued a health and safety advisory due to the sale of marijuana which failed laboratory testing. The products were sold between 12/27/2018 and 12/30/2018 at HG Lansing. This recall affects the following batches of flower sold from HG Lansing - License PC-000159 located at 1116 E. Oakland Ave., Lansing MI 48906.
Failed for E. coli and Salmonella
Failed for chemical residue
Failed for chemical residue and bile-tolerant gram-negative bacteria, E. coli, Salmonella and total coliforms
Failed for chemical residue and E. coli and Salmonella
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. Patients or caregivers who have these affected medical marijuana products in their possession should return them to HG Lansing for proper disposal. HG Lansing must notify patients or caregivers that purchased these medical marijuana products of the recall.
For more information about BMR, please visit www.michigan.gov/bmr
For more information about LARA, please visit www.michigan.gov/lara