Byron White FORMULAS A-FNG Herbal Supplement
Reason Label does not declare walnuts in English
ZOE brand Daily 30+ Prebiotic blend recall
Recalled by Zoe US, Inc. · Canton, MA, United States
Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.
Why it was recalled
Product may contain foreign objects: small metal pieces and/or stones
Hard or sharp fragments can cut the mouth or throat, break teeth or cause choking. They usually come from equipment wear or packaging on the production line. All foreign material recalls.
What was recalled
ZOE brand Daily 30+ Prebiotic blend; Dietary Supplement; 500g resealable pouch
Quantity: 142 units
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.
Expiration Date: 10/31/25 batch numbers: 24269, 24287, 24288
Where it was sold
Arizona California Colorado Connecticut District of Columbia Florida Georgia Hawaii Illinois Kentucky Massachusetts Maine Michigan Minnesota North Carolina New Jersey New Mexico New York Pennsylvania South Carolina Tennessee Texas Utah Virginia Washington Wisconsin
FDA's distribution note: Arizona, California, Colorado, Connecticut, District of Columbia, Florida, Georgia, Hawaii, Illinois, Kentucky, Maine, Massachusetts, Michigan, Minnesota, New Jersey, New Mexico, New York, North Carolina, Pennsylvania, South Carolina, Tennessee, Texas, Utah, Virginia, Washington, Wisconsin
Check the codes, then return or discard. Class II means eating it may cause temporary or reversible health problems. If your package matches the recalled codes, do not eat it - return it to the store or throw it away. 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
- Zoe US, Inc.
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Dec 4, 2024
- In FDA report of
- Jan 1, 2025
- Terminated
- Mar 3, 2025
- FDA recall number
- F-0316-2025 · event 95916
- Official record
- FDA enforcement report search
Recent dietary supplements recalls
All dietary supplements recallsByron White FORMULAS A-P Herbal Supplement
Reason Label does not declare walnuts in English
Byron White FORMULAS A-L Complex Herbal Supplement
Reason Label does not declare walnuts in English
Zen Principle Naturals Moringa Leaf Powder dietary supplement
Reason Possible Salmonella in Moringa Leaf Powder product.