Embargoed and Recalled Products

Vice Capital Extraction, LLC issued a voluntary recall on Tuesday, November 25, 2025, of pre-rolls that they produced.

The recall was prompted by marijuana flower that failed microbial testing and was then combined with other marijuana flower material, thereby contaminating the product.

Additionally, Vice Capital Extraction, LLC has emailed clients about the recall and will cover the disposal costs incurred by affected licensees.

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 a patient consumes any of the products mentioned and experiences an adverse health reaction, they should contact their physician immediately and fill out OMMA’s Health Impact Form. 

Processors that received the recall notice are required to inform dispensaries that bought the recalled products. Dispensaries must notify patients who purchased the recalled products and remove the items from shelves immediately. Licensees are responsible for disposing of recalled products per OMMA rules. Commercial licensees whose harvest or production batches are being recalled are responsible for disposal costs of all waste. 

• Product Recall: November 25, 2025
  • Recalled Product List

The Oklahoma Medical Marijuana Authority (OMMA) issued an embargo on Oct. 13, 2025, and a recall on Oct. 24, 2025, for products sold by Green Delight 2 LLC (DAAA-4JYA-UHMD).  

The products were recalled after failing for pesticides; 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 a patient consumes any of the products mentioned and experiences an adverse health reaction, they should contact their physician immediately and fill out OMMA’s Health Impact Form. 

Processors that received the recall notice are required to inform dispensaries that bought the recalled products. Dispensaries must notify patients who purchased the recalled products and remove the items from shelves immediately. Licensees are responsible for disposing of recalled products per OMMA rules. Commercial licensees whose harvest or production batches are being recalled are responsible for disposal costs of all waste. 

• Product Recall: October 24, 2025
  • Recalled Product List

OMMA issued an embargo on Oct. 13, 2025, and a recall on Oct. 23, 2025, for products produced by Ruby Mae’s LLC (PAAA-EKRQ-5DLS).   

The products were recalled for improper testing methods; 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 a patient consumes any of the products mentioned and experiences an adverse health reaction, they should contact their physician immediately and fill out OMMA’s Health Impact Form. 

Processors that received the recall notice are required to inform dispensaries that bought the recalled products. Dispensaries must notify patients who purchased the recalled products and remove the items from shelves immediately. Licensees are responsible for disposing of recalled products per OMMA rules. Commercial licensees whose harvest or production batches are being recalled are responsible for disposal costs of all waste. 

• Product Recall: October 23, 2025
  • Recalled Product List

The Oklahoma Medical Marijuana Authority (OMMA) issued an embargo on Sept. 25, 2025, and a recall on Oct. 10, 2025, for products produced by Michael William Redus DBA Rocking R Cannabis (PAAA-1H79-INUS).

• Product Recall: October 10, 2025
  • Recalled Product List

The Oklahoma Medical Marijuana Authority (OMMA) issued an embargo and recall on March 25, 2025, for multiple Payzos Flower & Buds, Grape Cream Cake Flower & Buds and Zour Apples Flower & Buds products due to the presence of heavy metals.

• Payzos Flower & Buds failed testing for arsenic.
• Grape Cream Cake Flower & Buds failed testing for cadmium.
• Zour Apples Flower & Buds failed for cadmium.

PAK Family Farm, LLC (GAAI-VYPS-KBZ2) contacted OMMA about testing concerns after producing the products. Their report led to an investigation by OMMA that revealed a similar test reporting issue by the same lab for Clever Leaf Outdoor, LLC (GAAA-VFSO-CG6V) products, prompting the embargo and recall. OMMA commends the efforts of both businesses to help swiftly remove these products from dispensary shelves. The collaboration was instrumental in protecting patient health and ensuring compliance.

• Product Recall: March 25, 2025
  • Recalled Product List

OMMA issued an embargo on June 7, 2024, and a Recall Notice on June 10, 2024. The listed products produced by Graves Farm Organics LLC (PAAA-EYKG-PCTX) failed re-testing for pesticides during an investigation.

• Product Recall: June 10, 2024
  • Recall Product and Business List

OMMA issued a recall notice on Nov. 3, 2023. The listed products were not properly tested by the processor in violation of OAC 442:10-8.

• Product Recall: Nov. 3, 2023
  • Recall Product and Business List

OMMA issued a recall notice on June 30, 2023, involving all infused prerolls, "Space Rocks - (g)" and "Space Rocks - Sativa" produced by Graves Farm Organics, LLC (PAAA-EYKG-PCTX), from Jan. 1, 2023 to June 20, 2023. The recalled products were not properly tested.

• Product Recall: June 30, 2023
  • Recall Product List
  • List of Dispensaries Affected

A licensee transferred medical marijuana products to other licensees after the products failed safety testing but before notifying OMMA of the failed tests, according to the Emergency Order of Embargo and Recall. 

Respondents to the Sept. 16, 2022, Emergency Order of Embargo and Recall shall use this form to request removal and disposal of subject medical marijuana products.

During routine lab inspections, OMMA discovered results that were not accurately reported by the testing lab. OMMA issued a recall notice on May 19, 2022.

• List of Recalled Products (May 19, 2022)

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.