The Oklahoma Medical Marijuana Authority (OMMA) issued a recall Tuesday for two medical marijuana flower production batches after testing identified excessive yeast and mold levels. The October 20 recall involves products from Blue Collar Criminals Collective, LLC, a licensed cultivation facility, and includes marijuana already distributed to dispensaries.
According to the state’s recall notice, the investigation began after the originating cultivation facility submitted a self-report and a licensed dispensary separately reported that certain flower batches had failed required testing after being transferred to retail locations.
OMMA’s Office of Investigation and Enforcement reviewed laboratory results and records from Metrc, Oklahoma’s marijuana inventory tracking system, confirming the affected products failed testing for total yeast and mold. Investigators subsequently traced the inventory to identify dispensaries that received the products and transactions involving medical marijuana patients.
The recall covers Biscotti and Smores Gelato flower sold under the BCC Legacy brand, including 3.5-gram packages, 7-gram and 14-gram smalls, and 2-gram sample products. The state’s official recall list identifies 31 affected package entries associated with the recalled batches.
Businesses identified in the recall records include Happa Wellness, Blue Collar Criminals Dispensary, S Pennsylvania Dispensary, P2P #1, Amador Holdings, Powerhouse Dispensary and Flavor Chasers Dispensary. The records also identify inventory held by the originating cultivation facility.
Alongside the recall, OMMA announced a new feature in Metrc designed to make recalled marijuana products easier for businesses to identify. Affected production batches and downstream packages will now display a warning symbol and a blue administrative recall alert within the inventory tracking system.
The agency said the feature takes effect immediately, with the October 20 recall serving as its first implementation. OMMA plans to use the same warning system for all future product recalls, giving licensed businesses a more visible indication when inventory has been flagged for safety concerns.
Patients who purchased affected products are advised not to consume them and should compare package information with the state’s published recall list. Products should be discarded or returned through the dispensary where they were purchased. Anyone experiencing an adverse health reaction should contact a physician and submit a report through OMMA’s Health Impact Form.
Licensed businesses must immediately remove recalled products from sale and notify affected downstream businesses and patients. Under Oklahoma regulations, the business responsible for the recalled production batches must cover disposal costs, while failure to comply with recall requirements can result in monetary penalties, license suspension or revocation.
