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FDA source record Class I Terminated

Mountain Meadow Herbs Brand Candida Flush Endotoxin Cleans3, 500 mg per capsule, 240 capsules per bottle. UPC 8 13086 01593 2. This product is sold as part of our Total Yeast ...

Recall Date: 2021-11-16 Recalling Firm: Mountain Meadow Herbs, Inc. Record Ref: F-0272-2022

FINDARECALL QUICK READ

What this record tells you

This FDA record concerns Mountain Meadow Herbs Brand Candida Flush Endotoxin Cleans3, 500 mg per capsule, 240 capsules per bottle. UPC 8 13086 01593 2. This product is sold as part of our Total Yeast ... and names Mountain Meadow Herbs, Inc. as the recalling firm. Use the source fields below to narrow the match, then verify the exact item and current remedy on the issuing-agency page.

  • Firm: Mountain Meadow Herbs, Inc.
  • Classification: Class I
  • Status: Terminated
  • Recall date: 2021-11-16
Best identifiers to check for a FDA record

Compare UPC/GTIN, lot or batch code, package size, flavor or variety, and any best-by/use-by date listed in the notice.

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Product Description & Identification

Mountain Meadow Herbs Brand Candida Flush Endotoxin Cleans3, 500 mg per capsule, 240 capsules per bottle. UPC 8 13086 01593 2. This product is sold as part of our Total Yeast Detox Package or it can be purchased separately.

Reason for Recall / Hazard Identified

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.

How to Check Whether Your Product Matches

A matching product name or photograph is not enough by itself. Compare every identifier available on your item or packaging with the official notice.

  1. Confirm the full product and brand or recalling-firm name.
  2. Compare package size, color, flavor, model, style, or configuration when listed.
  3. Check UPC, lot, batch, serial, date code, recall number, or USDA establishment number.
  4. Review the recall date and distribution information without assuming every seller is listed.
  5. Open the official FDA source below and follow its current instructions.

If a required identifier is missing, contact the recalling company or issuing agency through the official notice rather than guessing.

Consumer Action Recorded in the Source

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Distribution & Affected States

distributed in IN, KY, MN, MO, MT, NE, NY, OH, PA, TN, VA, and WI and in Ontario of Canada.

Verify With the Issuing Agency

This record was last updated in our index on 2026-08-09 21:59:13 UTC. Because recall enforcement statuses and instructions evolve, always verify details directly with the issuing government agency.

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Record Transparency

Issuing agency
FDA
Source ID
F-0272-2022
Indexed update
2026-08-09 21:59:13 UTC
Official source
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