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Alternative patient identification: To ensure timely access to medical marijuana, patients who have received application approval may now use their official OMMA approval email or approval in the OMMA MedPortal as a valid form of identification at licensed dispensaries. Read more here: UPDATE: Guidance on Alternative Patient ID

Product Recall: March 23, 2026

About

The Oklahoma Medical Marijuana Authority (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 is investigating to identify any related products that could be impacted; a notification will be shared as soon as new information is available. 

Information for Patients

Patients who believe they purchased impacted products should:

  1. Check products: Check the batch number on the product and compare it to the table provided below. 
  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 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.
  • 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.  
  • 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.

Recalled Product List

Recalled products are listed in the table below, which you can also download as a spreadsheet (.csv or .xlsx) or a searchable PDF.

The Oklahoma Medical Marijuana Authority (OMMA) issued an embargo on June 7, 2024, and a recall on June 10, 2024, involving products produced by Graves Farm Organics LLC (PAAA-EYKG-PCTX).

The recalled products failed safety re-testing for pesticides and include: Bomber pre-rolls, Orange Push Pop Crumble, Ice Cream Cake Crumble and Gorilla Breath Sugar. Bomber pre-rolls failed for the pesticide permethrin and Orange Push Pop Crumble, Ice Cream Cake Crumble and Gorilla Breath Sugar all failed for the pesticide spiromesifen.

The product recall list includes the product type, brand name, business name and date packaged. These products will be removed from shelves and properly disposed of according to OMMA rules, available at omma.ok.gov/rules.

Patients are advised to check the recall list o determine if any products currently on hand are impacted. If a patient is concerned about consuming a product listed, they are encouraged to contact their physician and fill out the Health Impact Form on OMMA's website at omma.ok.gov.

Processors that received the recall notice are required to inform dispensaries that bought the recalled products. Dispensaries are required to notify patients who purchased the recalled products and remove these items from shelves immediately.

Licensees must dispose of recalled products per OMMA rules. The commercial licensee whose harvest or production batch is being recalled is responsible for disposal costs of all waste. Licensees with questions are advised to visit omma.ok.gov/contact.

The cannabis recall process plays an important role in ensuring defective or potentially unsafe products are removed from the commercial market. Recalls are issued when OMMA scientists evaluate test results and other data leading to the determination that action is necessary. In many cases this includes submitting samples for multiple tests to confirm results, often utilizing multiple laboratories. With the passage of Senate Bill 813, authorizing OMMA to operate a quality assurance lab, this process will be expedited. Funding for the lab was secured in the most recent legislative session, and work is underway.

Recall Product and Business List

Recalled products are listed in the table below, which you can also download as a spreadsheet (.csv or .xlsx) or a searchable PDF.

FAQs

An embargo is a hold on specific product(s) that were found to:

  1. exceed the allowable testing thresholds set forth under our rules;
  2. contain analytes that could be poisonous, harmful to health or otherwise unsuitable or unsafe for human consumption;
  3. be in violation of applicable laws, rules or regulations.

Licensed businesses cannot engage in commercial activity (sale, donation, transfer, etc.) with embargoed products without the OMMA's permission. If your business is in possession of an embargoed product, you cannot send it to a waste facility (or other commercial license). You must await further instructions from the OMMA.

A recall takes place when the OMMA has ordered for the disposal of medical marijuana or medical marijuana products that have been sold to patients or caregivers AND meet at least one of the criteria below:

  1. exceed allowable testing thresholds set forth under our rules;
  2. are the subjects of an embargo or a derivative thereof;
  3. fail to meet standards set forth in our rules

The commercial licensee whose harvest or production batch is being recalled shall bear the costs for disposal of all medical marijuana waste.

After issuing the recall, dispensaries that have sold the product and the commercial licensee who grew or produced the product must assist in the recall in any way they can.

If you or your caregiver purchased a product from the above list, do not consume the product. Contact the dispensary for more information.

An embargoed product is in a holding pattern until the courts can determine whether OMMA has the authority to seize and destroy the product in question.

A recall occurs once we have confirmation that a product has been sold to patients and meets one of the below criteria:

1) exceeds allowable testing thresholds set forth under our rules;
2) is the subject of an embargo or a derivative thereof;
3) fails to meet the standards set forth in our rules.

Put another way, if a product has been embargoed, a business (including a dispensary) cannot engage in any commercial activity with that product. They can't sell it, distribute it, transport it, dispose of it, etc. They must also tag the product so it's obvious the product is under an embargo.

If a product has been recalled, the product needs to be destroyed and the businesses who have sold the product (either to patients or other businesses) are responsible for assisting with the recall in any way they can. Patients or caregivers who have purchased a recalled product need to contact the dispensary from which they bought the item to determine how they should move forward in assisting with the recall.

Patients are encouraged not to consume embargoed/recalled products.

Dispose of the product or contact the dispensary you purchased from. If a patient consumes any embargoed or recalled products and experiences an adverse health reaction, they should contact their physician immediately and fill out OMMA’s Health Impact Form.

If a business is selling a product that has been embargoed or recalled, please notify OMMA immediately via our complaint form.

Last Modified on Mar 23, 2026