(WWJ) It's another big pot recall by the state.
The Michigan Marijuana Regulatory Agency is recalling some medical marijuana vape products because of failed laboratory testing for high levels of Vitamin E Acetate — which health officials believe cause severe lung illness.
The recall affects some products sold at Fuel 420 in Jackson, the Green House of Walled Lake in Walled Lake, and The Green Mile Detroit; as well as Liv Wellness Center in Ferndale and the Vassar LLC in Vassar, Michigan.
This health and safety recall affects vape cartridges that were made before new emergency rules concerning vape products went into effect in November of last year.
All affected cartridges will have a label that indicates the license number of the marijuana facility that sold the marijuana product, as well as the METRC tag number assigned to the product in the statewide monitoring system.
The following products are included:
Fuel 420
This recall affects the following marijuana products sold from Fuel 420 – License PC-000077 – located at 1255 Falahee RD Jackson, MI 49203:
METRC # 1A4050100001AF5000000026Cart 510 .6G Wedding Cake - FUEL 420Sold between April 3, 2019 and November 11, 2019
METRC # 1A4050100001AF5000000032Carts 510 .6G Lime - FUEL 420Sold between March 31, 2019 and November 22, 2019
METRC # 1A4050100001AF5000000022Cart 510 .6G Skittlez - FUEL 420Sold between March 31, 2019 and November 22, 2019
METRC # 1A4050100001AF5000000031Carts 510 .6G Lemonade - FUEL 420Sold between March 31, 2019 and November 22, 2019
Green House of Walled Lake
This recall affects the following marijuana products sold from Green House of Walled Lake – License PC-000129 – located at 103 E. Walled Lake DR Walled Lake, MI 48390:
METRC # 1A40401000006A5000001961True-Green CrackSold between July 10, 2019 and November 22, 2019
METRC # 1A4050100000BB9000001101Motor City High | Green Crack | 1g CartSold between January 28, 2020 and February 5, 2019
METRC # 1A40401000006A5000001963True-SandferandoSold between July 20, 2019 and November 22, 2019
METRC # 1A4050100000BB9000001103Motor City High | San Fernando Valley | 1g CartSold between January 28, 2020 and February 5, 2019
METRC # 1A40401000006A5000001962True-North LightsSold between July 18, 2019 and November 22, 2019
METRC # 1A4050100000BB9000001102Motor City High | Northern Lights | 1g CartSold between January 28, 2020 and February 5, 2019
Liv Wellness Center, LLC
This recall affects the following marijuana products sold from Liv Wellness Center, LLC – License PC-000298 – located at 2625 Hilton Rd Suite 100 Ferndale, MI 48220:
METRC # 1A40401000006A5000002323True-Green CrackSold between September 18, 2019 and November 06, 2019
METRC # 1A40401000006A5000002325True-SandferandoSold between September 18, 2019 and November 21, 2019
METRC # 1A40401000006A5000002326True-North LightsSold between September 13, 2019 and November 06, 2019
METRC # 1A40401000006A5000002205True-CBD/THCSold between September 12, 2019 and November 19, 2019
The Green Mile Detroit
This recall affects the following marijuana products sold from The Green Mile Detroit – License PC-000144 – located at 6650 Eight Mile RD Detroit, MI 48234:
METRC # 1A40401000006A5000001527True-CBD/THCSold between June 8, 2019 and July 1, 2019
664 Vassar, LLC
This recall affects the following marijuana products sold from 664 Vassar, LLC – License PC-000035 – located at 664 State RD Vassar, MI 48768:
METRC # 1A40501000045ED000002619True-Green CrackSold between January 10, 2020 and February 4, 2020
METRC # 1A40501000045ED000002609True-SandferandoSold between January 10, 2020 and February 5, 2020
METRC # 1A40501000045ED000002620True-North LightsSold between January 10, 2020 and February 5, 2020
METRC # 1A40501000045ED000002618True-CBD/THCSold between January 10, 2020 and February 5, 2020
Patients or caregivers who have these affected vape cartridges in their possession should return them to the provisioning center where they purchased for proper disposal. The provisioning centers must notify patients or caregivers that purchased these vape cartridges of the recall, officiais said.
Patients who have experienced symptoms after using these products should report their symptoms and product use to their physician.
Patients and caregivers are asked to report any adverse product reactions to the MRA via email to MRA-Enforcement@michigan.gov, or via phone at 517-284-8599.