The Oklahoma Medical Marijuana Authority (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 on our website.
Patients who purchased these products should check their packaging/product label for the batch number listed in the table on our website. 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.
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 and/or investigators evaluate test results and other data, leading to the determination that action is necessary.
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