DETROIT (WWJ) - A recall has been issued for vape cartridges sold to medical marijuana patients in Detroit and Bay City.
The Marijuana Regulatory Agency says Vitamin E Acetate was found in several vape cartridges that failed safety compliance testing in December 2019 and February 2020. This recall also includes vape cartridges that did not have the required Vitamin E Acetate testing completed.
The cartridges were manufactured prior to the Emergency Rules for marijuana products filed on November 22, 2019.
All affected vape cartridges will have a label that indicates the license number of the marijuana facility that sold the marijuana product as well as tag number assigned to the product in the statewide monitoring system.
Patients who have experienced symptoms after using these products should report their symptoms and product use to their physician.
Patients and caregivers are requested to report any adverse product reactions to the MRA via email: MRA-Enforcement@michigan.gov or via phone: 517-284-8599.