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Product Recall: November 25, 2025

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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

Patients who purchased these products should check their packaging/product label for the batch number listed in the table on our website at omma.ok.gov/recall. 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.

Businesses

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 at omma.ok.gov/rules. Commercial licensees whose harvest or production batches are being recalled are responsible for disposal costs of all waste.

The cannabis recall process plays an important role in ensuring defective or potentially unsafe products are removed from the commercial market.   

Licensees with questions can use the contact form at omma.ok.gov/contact.

Statement from Vice Capital Extraction, LLC:

"To our Valued Patients and Customers:

Vice Capital Extraction, LLC is writing to inform you of a recent issue that arose during an inspection at our facility involving flower material that had failed harvest batch testing for microbials and has necessitatedthe undertaking of a voluntary recall.  The flower material that failed testing was combined with other flower material, thereby contaminating it, and then disseminated to vendors in pre roll form. 

Importantly, we immediately undertook an extensive internal inventory assessment of our processing facility and cooperated fully with OMMA as soon as this issue was discovered. We are actively working with the Authority to resolve the situation as patient safety has and will always remain our primary focus in this industry of uncertainty.

Out of an abundance of caution, we are notifying all recipients of pre-rolls associated with the contaminated flower material. The list of recalled products can be found on the OMMA website at: Recalled Product List

We respectfully request that you immediately remove any affected product from shelves and quarantine it until further notice. This is a voluntary recall done by Vice Capital Extraction with OMMA’s assistance. We will work with OMMA and licensees to ensure that the recalled products are properly disposed of or remediated at our expense. We are committed to transparency and will continue to provide updates as we receive further information or direction from OMMA.

If you have any questions or need assistance identifying the affected packages, please contact your sales rep or contact us directly at (405)212-9238.

We appreciate your understanding and commitment to maintaining the safety of medical marijuana products for Oklahoma patients. 

Sincerely, 
 
Vice Capital Extraction, LLC"

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.

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 Nov 25, 2025