Notification of Voluntary Product Recall  April 30, 2024 

Product Details

  • Product Type: Cannabis Topical
  • Product Description:  Mary’s Medicinal Transdermal Compound
  • Batch Number: MFC012424
  • UID Number: 1A4060300001AF7000002257
  • Packaged by: RCW Manufacturing
  • Date packaged (Pkg): After February 8, 2024
  • Locations Sold: Multiple, see website for list
  • Dates Sold: After February 13, 2024
Learn more about this recall

Consumers 

If you purchased this product:

  • If you are experiencing symptoms or any adverse reactions, contact your physician immediately.
  • Check your package for the UID or batch numbers included in this recall.
  • If the UID or batch number matches, dispose of the product or return it to the retailer for proper disposal.

Licensees 

DCC and/or the Distributor will send email notices to all licensees with a recalled product in their inventory with instructions. If you have questions, or need additional information, please contact [email protected].gov

Learn more about cannabis recalls

The cannabis recall process plays an important role in ensuring defective or potentially unsafe products are removed from the market. The DCC maintains a list of both DCC-mandated and voluntary recalls.

View all cannabis recalls

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