Stop using nowFood recall · FDA · Published November 16, 2021
Mountain Meadow Herbs Recalls Candida Flush Due to Pressurized Bottle Hazard
Mountain Meadow Herbs recalls Candida Flush Endotoxin Cleans3 because bottles may become pressurized, risking injury from expelled contents upon opening.
Product bottle has potential to become pressurized over time. When consumer opens a bottle, the cap, capsules, and product powder could be forcefully expelled, and customers may sustain injuries to their hands and eyes.
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Contact the company
📍Recalling firmMountain Meadow Herbs, Inc.1019 Hard Rock Rd · Somers, MT 59932-9792
✎ GovInfoNow plain-language explainer
Mountain Meadow Herbs, Inc. is recalling its Candida Flush Endotoxin Cleans3 supplement because the product bottles have the potential to become pressurized over time. If a consumer opens a bottle, the cap, capsules, and powder could be forcefully expelled, potentially causing injuries to hands and eyes. The recall affects 54 bottles distributed in several U.S. states and Ontario, Canada. Read more at govinfonow.com/recall/13726-mountain-meadow-herbs-recalls-candida-flush-due-to-pressurized-bottle.
“Mountain Meadow Herbs Recalls Candida Flush Due to Pressurized Bottle Hazard.” GovInfoNow, updated October 10, 2026. https://govinfonow.com/recall/13726-mountain-meadow-herbs-recalls-candida-flush-due-to-pressurized-bottle. Based on FDA recall #F-0272-2022 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-0272-2022%22&limit=1).
The FDA announced on November 16, 2021, that Mountain Meadow Herbs, Inc. voluntarily recalled its Candida Flush Endotoxin Cleans3 supplement due to potential pressurization hazards. The agency said the recall affects 54 bottles distributed in several U.S. states and Ontario, Canada.
The FDA said the product bottle has potential to become pressurized over time. When a consumer opens a bottle, the cap, capsules, and product powder could be forcefully expelled, potentially causing injuries to hands and eyes.
Context
GovInfoNow's records show other recent recalls of similar products include Lotus Vaping Monarch Premium Kratom Green Maeng Da Powder Recall (2025-10-30), Diva Fam Sea Moss Gel Superfood Recall (2026-01-09), and Pure Ground Ingredients Recalls Organic Peppermint Leaf Powder Due to Salmonella Risk (2026-04-08).
How to tell if you have this one
Check for Mountain Meadow Herbs Brand Candida Flush Endotoxin Cleans3, 500 mg per capsule, in a bottle containing 240 capsules. Look for UPC 8 13086 01593 2. The specific recalled lot is #0120011Q.
Brand
Mountain Meadow Herbs
Product
Mountain Meadow Herbs Brand Candida Flush Endotoxin Cleans3, 500 mg per capsule, 240 capsules per bottle. UPC 8 13086
Category
Food
Based on the official FDA remedy
What to do — step by step
Stop Using the Product
Do not open or consume the product due to the risk of pressurized expulsion causing injury.
Contact the Manufacturer
Reach out to Mountain Meadow Herbs, Inc. for further instructions on the recall remedy.
Where it went and when
Where it was distributed
Distributed in 12 states, and outside the U.S.
Listed by the agency
Not listed
FDA distribution: “distributed in IN, KY, MN, MO, MT, NE, NY, OH, PA, TN, VA, and WI and in Ontario of Canada.” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: Indiana, Kentucky, Minnesota, Missouri, Montana, Nebraska, New York, Ohio, Pennsylvania, Tennessee, Virginia, Wisconsin.
Recall timeline
FDA terminated this recall 56 days after the firm started it.
1Firm started the recall
2FDA classified it Class I
3Published in FDA’s Enforcement Report
4FDA terminated the recall
Dates from the agency record only; steps without a date are left out.
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
Official source: FDA Recall #F-0272-2022 (November 16, 2021) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-0272-2022 to see it in context.
Plain-language summary written by qwen3.6:35b-a3b on October 10, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.