Byron White FORMULAS A-FNG Herbal Supplement
Reason Label does not declare walnuts in English
Mountain Meadow Herbs Brand Candida Flush Endotoxin Cleans3 recall
Recalled by Mountain Meadow Herbs, Inc. · Somers, MT, United States
Class I — High risk. Reasonable probability of serious harm or death.
Why it was recalled
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.
See the recall's own reason text for the specifics. All other reasons recalls.
What was recalled
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.
Quantity: 54 bottles
Food: Dietary supplements
Lot codes, dates and UPCs
A recall covers only these codes. Compare them with the lot number, best-by date or UPC printed on your package.
***Exp 12/22. Expiration Date: 12/20200 ***Lot #0120011Q.
Where it was sold
Indiana Kentucky Minnesota Missouri Montana Nebraska New York Ohio Pennsylvania Tennessee Virginia Wisconsin
FDA's distribution note: distributed in IN, KY, MN, MO, MT, NE, NY, OH, PA, TN, VA, and WI and in Ontario of Canada.
Do not eat it. Class I means FDA judged there is a reasonable probability of serious illness or death. If the brand, size and lot or date code on your package match, throw the product away or return it to the store for a refund, and clean any surface or container it touched. If anyone has eaten it and feels unwell, contact a doctor and mention the recall. FDA lists this recall as terminated: the company has finished removing the product, so it should no longer be on shelves - but it can still be in a freezer or pantry.
- Recalling firm
- Mountain Meadow Herbs, Inc.
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Nov 16, 2021
- In FDA report of
- Dec 15, 2021
- Terminated
- Jan 11, 2022
- FDA recall number
- F-0272-2022 · event 89066
- Official record
- FDA enforcement report search
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