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Product Recall: June 10, 2024

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

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.

The reason a product is recalled is listed in the table above. In general, it is not advisable that a patient use or consume a product listed in the table above.

If you or a caregiver has purchased a product that is now recalled, please contact the dispensary from which you bought the product for further instructions.

If a business is selling a product that has been recalled, please notify the OMMA immediately through our complaint form.

Last Modified on Jun 20, 2024