← FDA ENFORCEMENT
F-0316-2025Class II

Zoe US, Inc.

What this record is not

A recall record is reproduced as FDA published it, and the classification is FDA’s. SPEQ adds no interpretation, and a recall concerns the products and dates in the record — it is not a statement about a company’s other products or its current status.

Recalling firm
Zoe US, Inc.
Product type
Food / supplement / cosmetic
Status
Terminated
Report date
2025-01-01
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
Firm state
MA
Product quantity
142 units
Initiated by
Voluntary: Firm initiated
SPEQ quality domain
Environmental Monitoring
Reason for recall

Product may contain foreign objects: small metal pieces and/or stones

Product description

ZOE brand Daily 30+ Prebiotic blend; Dietary Supplement; 500g resealable pouch

Code / lot info

Expiration Date: 10/31/25 batch numbers: 24269, 24287, 24288

Other recalls SPEQ maps to Environmental Monitoring
See all Environmental Monitoring recalls →

Data: U.S. FDA. Recall details are as reported by the FDA. The quality-domain mapping and severity are a SPEQ editorial interpretation of the recall reason, not an official FDA classification. Open the enforcement explorer →