Class IITerminatedVoluntary: Firm initiated
Zoe US, Inc.: food recall F-0316-2025
Zoe US, Inc. of Canton, MA recalled ZOE brand Daily 30+ Prebiotic blend; Dietary Supplement; 500g resealable pouch. Reason: Product may contain foreign objects: small metal pieces and/or stones. The FDA listed it as Class II in its Enforcement Report dated Jan 1, 2025; distribution: 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.
Record status as published: Terminated (terminated Mar 3, 2025). openFDA data last updated Oct 21, 2026.
Have this product? Check FDA.gov and your retailer. This page reproduces an FDA Enforcement Report record and is not a public alert. Look for the firm's recall notice on the FDA's recalls page, or ask the store where you bought it what to do. If you think you got sick from a food, contact a health care provider.
Recall details
- Product
- ZOE brand Daily 30+ Prebiotic blend; Dietary Supplement; 500g resealable pouch
- Product quantity
- 142 units
- Reason for recall
- Product may contain foreign objects: small metal pieces and/or stones
- Codes, lots and dates on the package
- Expiration Date: 10/31/25 batch numbers: 24269, 24287, 24288
- Distribution pattern
- 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
- Recalling firm
- Zoe US, Inc., Canton, MA
- Classification
- Class II — the FDA uses this class for a situation in which using or being exposed to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious adverse health consequences is remote.
- Voluntary or mandated
- Voluntary: Firm initiated
- How the firm first notified customers
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Dates
| Event | Date |
|---|---|
| Recall initiated by the firm | Dec 4, 2024 |
| Classified by the FDA | Dec 24, 2024 |
| Published in the Enforcement Report | Jan 1, 2025 |
| Terminated | Mar 3, 2025 |
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Sources
- U.S. Food and Drug Administration, openFDA food enforcement reports, recall number F-0316-2025 (openFDA record). Data provided by the U.S. Food and Drug Administration (https://open.fda.gov).
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