F-0316-2025
Zoe US, Inc.
Data retrieved 2026-10-27T22:06:49.008Z
Site-assigned category (for this product recall): Contamination
Independent website; not affiliated with or endorsed by FDA. Recall information is attributed to the linked FDA record. Categories are assigned by this website using keyword rules; they are not FDA classifications or independent legal findings and may be incomplete or incorrect. A category summarizes the stated reason for the identified product recall, not a finding about the firm generally or its other products. FDA’s original reason text appears below.
Official openFDA record · FDA recalls and safety alerts
Fields as reported by FDA
Dates are formatted YYYY-MM-DD. “Not reported” means the field was absent or empty.
- recall_number
- F-0316-2025
- event_id
- 95916
- recalling_firm
- Zoe US, Inc.
- city
- Canton
- state
- MA
- country
- United States
- product_description
- ZOE brand Daily 30+ Prebiotic blend; Dietary Supplement; 500g resealable pouch
- reason_for_recall
- Product may contain foreign objects: small metal pieces and/or stones
- classification
- Class II
- FDA-reported status (not current status)
- Terminated
FDA does not update this status after recall classification. It may not reflect whether the recall is currently ongoing, completed, or terminated. - voluntary_mandated
- Voluntary: Firm initiated
- 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
- product_quantity
- 142 units
- code_info
- Expiration Date: 10/31/25 batch numbers: 24269, 24287, 24288
- recall_initiation_date
- 2024-12-04
- report_date
- 2025-01-01
- termination_date
- 2025-03-03