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Oklahoma City, OK The Oklahoma Medical Marijuana Authority is expanding a recall initiated on March 23, 2026, for certain medical products processed by Sunny Roads Processing 2, LLC (PAAA-8JA2-CK1Z). As shared in the original notice OMMA continued it investigation to determine whether related products were affected. Based on those findings, the recall has expanded to include additional items.
Oklahoma City, OK Oklahoma licensed medical marijuana dispensaries wanting to register under the new federal resistration requirements, the U.S. Drug Enforcement Administration (DEA) have published intrusctions for submitting the required data in it application.
Commercial licensees who choose not to participate may continue to operate in accordance with the existing regulatory framework in Oklahoma, however you will not be eligible to benefit on potential tax breaks, banking services or inter
OMMA has issued a recall for several medical marijuana pre-roll batches processed by Sunny Roads Processing 2, LLC (PAAA-8JA2-CK1Z). OMMA received reports of concerns about pre-rolls purchased at Miami Natural Health, LLC. The reports resulted in immediate testing of the products at multiple labs; the products failed testing due to pesticide content above allowable thresholds. OMMA then conducted product tracing to determine that Sunny Roads Processing 2, LLC processed the affected pre-rolls.
OMMA has issued a mandatory recall for medical marijuana products tested by Greenleaf Labs LLC (LAAA-MP4O-T1EE) between April 2023 and July 2025. This action follows a previous emergency order establishing product safety concerns that remain unresolved by the licensee. In August 2025, OMMA ordered Greenleaf Labs to cease operations after a routine inspection revealed testing inaccuracies.
OMMA issued an embargo on Jan. 21, 2026, for products processed and/or labeled by OK Farms (PAAA-FQG6-QLJP) and RX Harvest Botanicals (PAAA-F0B4-WJQP). These facilities are not legal operators, and the license numbers were not issued by OMMA.
The products were discovered at Bud Guys LLP (DAAA-X7XP-Q2J9) dispensary in Tulsa. Because the products were not tagged in the state inventory tracking system, testing of the products cannot be confirmed.
OMMA issued an embargo on Dec. 11, 2025, and a recall on Dec. 23, 2025, for products derived from concentrates originating from Carter County Extracts, Inc. (PAAA-NKNM-0GP0).
The products were recalled after failing for pesticides (Myclobutanil); view the full product table below.
Patients who purchased these products should check their packaging/product label for the batch number listed in the table. If the numbers match, dispose of the product or contact the dispensary you purchased from. If
Oklahoma medical marijuana industry employees must submit a renewal application for their OMMA-issued credential required by law. All renewal applications must be submitted a year after approval of the previous application.
To renew or apply for a credential, you must log in to the licensing portal.
Owners are not required to have a credential. Consultants who are responsible for the duties outlined in the definition of "employee" per Senate Bill 1704 and OMMA Rules in 10-5-1(13)(A) should be
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