Recall archive / FDA food enforcement
ZOE brand Daily 30+ Prebiotic blend; Dietary Supplement; 500g resealable pouch — FDA record F-0316-2025
Reported terminated
Status as reported in the agency record. FDA warns that enforcement status may not track the current recall lifecycle; check the current official notice.
Source date Dec 4, 2024. Retrieved Oct 1, 2026. Last updated Oct 1, 2026.
Archive changed Oct 1, 2026. USDA FSIS records are unavailable; check FSIS directly. Source coverage and dates.
What the record says
- Product
- ZOE brand Daily 30+ Prebiotic blend; Dietary Supplement; 500g resealable pouch
- Reason
- Product may contain foreign objects: small metal pieces and/or stones
- Classification
- Class II
- Recalling firm
- Zoe US, Inc.
- Quantity
- 142 units
- Agency-reported status
- Terminated
- Source record identifier
- F-0316-2025
What the recall classes mean. Classification is an agency assessment, not individual medical advice.
Lot and product identifiers
| Label field | Details supplied by the agency |
|---|---|
| Lot, code or applicability | Expiration Date: 10/31/25 batch numbers: 24269, 24287, 24288 |
Match all identifying details in the current notice. A brand name alone is not enough.
Distribution
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
States below are derived from the distribution text, including nationwide wording. They are not inferred from the firm's address.
Dates in the source
- Report date
- Jan 1, 2025
- Recall initiation date
- Dec 4, 2024
- Center classification date
- Dec 24, 2024
- Termination date
- Mar 3, 2025
FDA company pages use the listing date; enforcement records use initiation dates; CPSC uses recall date; NHTSA uses report-received date. These dates are not interchangeable.