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). 

1. Check products: Check the batch number on the product and compare it to the table on the OMMA Recalls page.
2. Contact the dispensary: Patients should dispose of recalled products or contact the dispensary where the item was purchased. 
3. Monitor health: If patients experience an adverse reaction after consuming an impacted product, contact your physician immediately and complete OMMA's Health Impact Form.  
4. Report violations: Patients who see recalled products on shelves are encouraged to submit a tip via OMMA's Business Complaint Form. 

• 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.