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).
The products were recalled for improper testing methods; the product list includes: Assassin Infused Pre-Rolls, Black Runtz Pre-Rolls, Black Truffle Pre-Rolls, Blackberry Octane Pre-Rolls, Blueberry Muffin 57 Pre-Rolls, Blueberry Muffin Pre-Rolls, Bruce Banner Pre-Rolls, Bruce Banner ½ gram Pre-Rolls, Chiesel Pre-Rolls, Chocolate Mint Grenades, Crown Royal Pre-Rolls, Dank Tank Pre-Rolls, Dank Tank Mini Pre-Rolls, Fruity Pebbles OG Pre-Rolls, Future Ex Pre-Rolls, Gelato 33 Pre-Rolls, Gelato 41 Pre-Rolls, Gelato 45 Pre-Rolls, GG4 Pre-Rolls, Gorilla Glue Pre-Rolls, Grape Gas Pre-Rolls, Grape Gelato Pie Pre-Rolls, Guapa Pre-Rolls, Gumbo Kush Pre-Rolls, Ice Cream Cake ½ gram Pre-Rolls, Ice Cream Cake Pre-Rolls, Italina Ice Pre-Rolls, Jungle Cake Pre-Rolls, Killer Cupcake Pre-Rolls, King Runtz Pre-Rolls, Lemon Cherry Gelato Pre-Rolls, MAC 1 Pre-Rolls, Mac and Cheese Pre-Rolls, Mac Pre-Rolls, Magic Mike ½ gram Pre-Rolls, Magic Mike Pre-Rolls, Mochi Mousse Pre-Rolls, Northern Lights Pre-Rolls, Obama Runtz ½ gram Pre-Rolls, Obama Runtz 2 Pre-Rolls, Obama Runtz Pre-Rolls, OG Kush 1g (Hybrid) Vape Cartridges, Orange Gelato 1g (Hybrid) Vape Cartridges, Oreoz Pre-Rolls, Pineapple Express Punch 1g (Hybrid) Vape Cartridges, Purple Kush 1g (Hybrid) Vape Cartridges, Purple Princess 2 Pre-Rolls, RRC 1 gram Pre-Rolls, RS-11 Pre-Rolls, Runtz ½ gram Pre-Rolls, Runtz Pre-Rolls, Space Fuel Pre-Rolls, Strawberry Mac Pre-Rolls, Super Runtz Pre-Rolls, Sweet Killer Pre-Rolls, Tropicana Banana Pre-Rolls, White Truffle ½ gram Pre-Rolls, White Truffles Pre-Rolls and White Truffles 2 Pre-Rolls.
The full recall list is available at omma.ok.gov/recall. The list includes the product type, brand name, business name and date packaged. Licensees must dispose of recalled products following OMMA Rules.
Patients are advised to check the recall list to determine if any products they have on hand are impacted. If a patient is concerned about consuming a product listed, they are encouraged to contact their physician 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 are required to notify patients who purchased the recalled products and remove these items from shelves immediately.
The commercial licensee whose harvest or production batch is being recalled is 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.
Licensees with questions are advised to visit omma.ok.gov/contact.
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