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Oct. 20, 2026
Recall Issued for Flower Grown by Blue Collar Criminals Collective, LLC (GAAI-NJVE-0Z9P)
OKLAHOMA CITY, OK — The Oklahoma Medical Marijuana Authority (OMMA) has issued a recall for two medical marijuana flower production batches from Blue Collar Criminals Collective, LLC. (GAAI-NJVE-0Z9P) licensed grow facility.
OMMA received a self-report from the originating grow facility and a report from a licensed dispensary, indicating that specific flower production batches had failed required testing after being transferred to dispensaries.
OMMA’s Office of Investigation and Enforcement (OIE) reviewed laboratory results and Metrc tracking data, confirming the affected product batches failed testing for yeast and mold. The OIE team then traced all affected inventory to identify each receiving dispensary and patient transaction.
A complete list of recalled products and batch numbers is available on our website.
Metrc Update: How Recalled Products Will Now Appear in Your Inventory
OMMA has implemented a new visual inventory flag in Metrc to streamline how recalled products are identified in the supply chain. Affected production batches and downstream packages will now be highlighted with a warning symbol and a blue administrative recall alert message.
 This feature is effective immediately and applies to today’s issued recall. Licensees holding affected inventory will see these flags in Metrc today. OMMA will use this flagging process for all future product recalls.
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Recall Information for Patients
Patients who believe they purchased impacted products should:
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Check products: Check the batch number on the product and compare it to the table on the OMMA Recalls page.
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Contact the dispensary: Patients should dispose of recalled products or contact the dispensary where the item was purchased.
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Monitor health: If patients experience an adverse reaction after consuming an impacted product, contact your physician immediately and complete OMMA's Health Impact Form.
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Report violations: Patients who see recalled products on shelves are encouraged to submit a tip via the OMMA Business Complaint Form.
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Required Recall Actions for Commercial Licensees
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Commercial licensees are responsible for notifying any impacted downstream businesses and patients. Dispensaries should remove the recalled products from shelves immediately; these products cannot legally be sold to patients.
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Recalled products must be disposed of in accordance with OMMA rules. The licensee whose harvest or production batches are being recalled bears responsibility for disposal costs of all waste.
- The recall process plays an important role in ensuring defective or potentially unsafe products are removed from the commercial market. Recalls are issued when OMMA evaluates test results and other data, leading to the determination that action is necessary.
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Licensees with questions can reach OMMA via the contact form.
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Pursuant to OAC 442:10-8-1(g)(2)(C)(vi), a licensee’s failure to timely comply with recall provisions may result in revocation, suspension and monetary penalties.
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