CONSUMER + ACCOUNTABILITY · National ·
6 States. 8 Recalls. THC at 133x the Legal Limit. A Lab That Lied for Two Years. And Untested Flower at Nine Ohio Dispensaries.
Every Monday (or Tuesday, let’s be honest), CWR checks every major US state cannabis regulatory agency to compile every active recall. Use our weekly list to check your products and check your batch numbers. Here’s what regulators flagged this week.
🔴 MINNESOTA — Tidal Wave Vapes (Hemp)
Issued: March 18, 2026 · Recall type: Mandatory · Reason: THC content up to 133x legal label amount · Risk: High
The Minnesota Office of Cannabis Management recalled all flavors of Tidal Wave brand 3.5-gram disposable vapes, distributed by Ocean Wholesale LLC. Products labeled as containing less than 0.3% THC actually tested between 13.5% and 40.7%. Thats up to 133 times the stated amount! These were sold through hemp shops, tobacco stores, and online retail – not licensed dispensaries – and carry no lot numbers, making full recall verification nearly impossible. Discard immediately. If you feel ill: Minnesota Poison Control 1-800-222-1222. Report at cannabis.mn.gov.
🔴 OHIO — Modern Flower Minis Flower White Truffle (Failed Pre-Sale Testing)
Issued: March 16, 2026 · Recall type: Class II · Reason: Product samples not properly tested before sale · Risk: Remote but unverified
Ohio’s Division of Cannabis Control issued a Class II recall for 5.66-gram Modern Flower Minis Flower White Truffle, cultivated by Harvest Grows, LLC. The products were sold before completing required safety testing. A Class II recall means a remote possibility of adverse effects — no illnesses have been reported — but the products are non-compliant and must be removed. Affected products were sold at nine dispensaries including Ohio Cannabis Company in Piqua and Trulieve locations in Columbus, Zanesville, Cincinnati, Lorain, and Findlay. Check your batch number against the full DCC list at com.ohio.gov/divisions/cannabis-control. Return to your dispensary for a refund.
🔴 ARIZONA — Legacy & Co. Cheech & Chong Infused Preroll (Aspergillus)
Issued: March 18, 2026 · Recall type: Voluntary · Reason: Possible Aspergillus fungal contamination · Risk: Elevated for immunocompromised patients
The Arizona Department of Health Services issued a voluntary recall for the Legacy & Co. Cheech & Chong Infused Preroll 3pk 1g Apple Fritter, batch number K-2025-C3P3-AFRI, licensed through JARS Cannabis dispensaries. Aspergillus is a fungus that can cause serious infection in people with weakened immune systems or underlying lung conditions. No illnesses reported. Products are quarantined at point of sale pending confirmatory testing. Do not use this batch. Contact your dispensary for disposal or refund.
🔴 OKLAHOMA — Sunny Roads Processing 2, LLC (Pesticides)
Issued: March 23, 2026 · Recall type: Mandatory · Reason: Pesticide content above allowable thresholds · Risk: Moderate to high
OMMA issued a mandatory recall for multiple pre-roll batches processed by Sunny Roads Processing 2, LLC (license PAAA-8JA2-CK1Z) after consumer complaints at Miami Natural Health, LLC triggered multi-lab testing, all confirming pesticides above threshold. OMMA is still tracing additional affected products. Full batch number list at oklahoma.gov/omma/recalls. If you experience adverse effects, complete OMMA’s Health Impact Form and contact your physician.
🔴 OKLAHOMA — Greenleaf Labs LLC (Mandatory Recall / Testing Fraud)
Issued: March 19, 2026 · Recall type: Mandatory · Reason: Lab reported inaccurate yeast and mold results for two years, ~19,000 samples · Risk: High — scope is massive, products still being found on shelves
The most serious active recall in the country right now. OMMA issued a mandatory recall covering all medical cannabis products tested by Greenleaf Labs LLC between April 2023 and July 2025. The lab was miscalculating mold and yeast content for over two years, affecting approximately 19,000 samples. OMMA shut the lab down in August 2025. Despite a voluntary retesting commitment, OMMA compliance inspectors are still finding test-failed products on dispensary shelves in 2026. If you are an Oklahoma medical cannabis patient who purchased products during this window, check your batch numbers against the recall table at oklahoma.gov/omma/recalls.
🔴 COLORADO — Timberline Extracts (Chlorfenapyr Pesticide)
Issued: March 20, 2026 · Recall type: Health and Safety Advisory · Reason: Chlorfenapyr pesticide above legal limits · Risk: Moderate
Colorado’s Marijuana Enforcement Division issued a Health and Safety Advisory for concentrate from Timberline Extracts (David Jackson LLC), distributed to 32 dispensaries statewide and sold between September 4, 2025, and March 10, 2026. Chlorfenapyr is a banned insecticide that disrupts cellular energy production – it is not safe for human consumption. This is Colorado’s 8th cannabis recall of 2026 and its 15th since November 2025. Chlorfenapyr has now appeared in at least 10 Colorado advisories since June 2025, pointing to a systemic contamination problem in Colorado’s supply chain that state regulators have yet to fully address. Return or destroy affected products. Full dispensary list at med.colorado.gov.
🟡 Maine — MarijuanaVille Medical Cannabis Patient Advisory (Multiple Pesticides)
Issued: January 22, 2026 · Type: Patient Advisory (not a recall, read below) · Reason: Multiple pesticides at unsafe levels in medical cannabis concentrates · Risk: High for medical patients
This entry deserves its own explanation. Maine’s Office of Cannabis Policy issued a patient advisory — not a recall — for five strains of medical cannabis concentrates sold at MarijuanaVille: Denty Honey, Orange Kush Breath, Pineapple Mimosa, Raw Honey, and Sexy Sally. Testing showed varying unsafe levels of multiple pesticides following a patient complaint about an adverse health reaction.
Here is why this matters beyond the specific products: Maine law does not give OCP the authority to issue mandatory recalls in the medical cannabis program. It can only issue advisories. So when a medical cannabis patient in Maine buys a contaminated product, the state cannot legally force a recall. It can only advise. Maine is currently the only state where medical cannabis is not required to be tested at all. A bill to change that is moving through the legislature right now. If you purchased any of these products, do not use them. Contact your dispensary or caregiver. If you are experiencing symptoms, call your doctor or dial 911.
🟡 NEW YORK — Keystone State Testing NY (Still Active / Lab Fraud)
Issued: February 26, 2026 · Status: Still active; included for ongoing consumer awareness · Reason: Lab issued unreliable results; 54 lots with misreported Aspergillus, 1 lot with misreported cadmium · Risk: High
The New York Office of Cannabis Management issued this recall on February 26 and it remains active this week. Following a December–January audit, OCM found that Keystone State Testing New York issued unreliable test results for 55 product lots, 54 with incorrectly reported Aspergillus mold results and one with misreported cadmium levels. All 55 lots are considered adulterated. Multiple licensees are affected across a wide range of flower, pre-roll, and concentrate products. Full lot-by-lot list at cannabis.ny.gov/current-recalls. Return to the dispensary where you purchased for a full refund.
What to do if you have a recalled product
- Stop using it immediately: Contact the dispensary where you purchased it, and ask them how to dispose of it safely.
- Check your batch number: Every recall above includes a specific batch or lot number. Look at the product label and cross-reference with the state agency links provided.
- Report adverse effects right away: Its important to contact your doctor and Poison Control as well: 1-800-222-1222 (national, 24/7).
- File a complaint with your state agency: Easily find and contact your state cannabis regulatory body on our State-By-State resources map! Seperate links are listed above for each recall. Your report can help regulators trace affected products faster and (in theory) create a safer industry.
The bigger picture this week
Two of this week’s eight recalls are lab fraud cases – Greenleaf Labs in Oklahoma and Keystone State Testing in New York – where testing laboratories misreported results that products had passed. This is the baseline failure that sits underneath every other failure in the legal cannabis system. Product testing is the last line of defense before a product reaches a consumer. When the lab is the problem, the entire chain collapses. Safety by definition cannot exist when the main checkpoint for product quality is fraudulent itself.
Illinois, for context, has issued zero public cannabis recalls in the history of its program. Not because its products are cleaner, but because the state handles contamination complaints through confidential administrative processes that don’t reach consumers. Historically, self-regulation does NOT work in favor of the consumer.
CWR checks every major state regulatory agency each week. If a state isn’t on this list, it either had no active recalls or doesn’t maintain a public recall page. We’ll note which is which to keep you in the loop!
Sources: KSTP / MN OCM · Ohio DCC / Columbus Today · FOX 10 / AZ ADHS · OMMA — Sunny Roads · OMMA — Greenleaf Labs · Colorado MED · NY OCM Current Recalls · California DCC Recalls Portal · Michigan CRA Public Health Bulletins · Washington LCB Recalls · Illinois IDFPR Annual Cannabis Report 2025
Know about a recall we missed? Contact CWR.
