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Marijuana Products Recalled in Lansing

Media Contact: LARA Communications 517-373-9280
Email: mediainfo@michigan.gov

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.

Citrix
1A4050100000F3D000000009
Failed for E. coli and Salmonella

Gelato
1A4050100000F3D000000010
Failed for chemical residue

Green Crack
1A4050100000F3D000000008
Failed for chemical residue and bile-tolerant gram-negative bacteria, E. coli, Salmonella and total coliforms

Oreoz
1A4050100000F3D000000023
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