OKLAHOMA CITY, OK — The Oklahoma Medical Marijuana Authority (OMMA) is expanding a recall initiated on March 23, 2026, for certain medical marijuana products processed by Sunny Roads Processing 2, LLC (PAAA-8JA2-CK1Z).
As shared in the original notice, OMMA continued its investigation to determine whether related products were affected. Based on those findings, the recall has been expanded to include additional items.
March 23: Recalled products list
May 15: Expanded recalled products list
Information for Patients
Patients who believe they purchased impacted products should:
- Check products: Check the batch number on the product and compare it to the table provided below.
- Contact the dispensary: Patients should dispose of recalled products or contact the dispensary where the item was purchased.
- Monitor health: If patients experience an adverse reaction after consuming an impacted product, contact your physician immediately and complete OMMA's Health Impact Form.
- Report violations: Patients who see recalled products on shelves are encouraged to submit a tip via the OMMA Business Complaint Form.
Required Actions for Commercial Licensees
- 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.
- 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.
- Licensees with questions can reach OMMA via the contact form.
- 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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Last Modified on
May 15, 2026
