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Notification of Medical Marijuana Product Recall for Plan B Wellness

Media Contact: LARA Communications 517-335-LARA (5272)

May 14, 2020 – The Marijuana Regulatory Agency (MRA) issued a health and safety advisory bulletin today due to the presence of Vitamin E Acetate in several vape cartridges which failed safety compliance testing in April 2020. These cartridges were manufactured prior to the Emergency Rules for marijuana products intended for inhalation 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.

This recall affects the following marijuana products sold from Plan B Wellness – License PC-000137– located at 20101 8 Mile RD, Detroit, MI 48219:

Package #1A405010000426A000000095 (Royal Highness Vape Cart 1G)
Sold between October 13, 2019 and November 22, 2019

Patients or caregivers who have these affected vape cartridges in their possession should return them to Plan B Wellness for proper disposal. Plan B Wellness must notify patients or caregivers that purchased these vape cartridges of the recall.

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: or via phone: 517-284-8599.

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