Food recall

Zoe US, Inc. recall: ZOE brand Daily 30+ Prebiotic blend

Zoe US, Inc., of Canton, MA, recalled ZOE brand Daily 30+ Prebiotic blend. The FDA's reason: “Product may contain foreign objects: small metal pieces and/or stones.” The FDA classified it Class II: it could cause temporary or minor harm. The company began the recall voluntarily on December 4, 2024, and the FDA first listed it in its Enforcement Report of January 1, 2025. The FDA has closed the recall: it found the company did all it reasonably could to remove or correct the product.

How serious

Class II

It could cause temporary or minor harm

Why

Metal, plastic, glass or other objects

Status

Terminated

Closed March 3, 2025

The recall

Company
Zoe US, Inc. (Canton, MA)
Reason, in FDA's words
“Product may contain foreign objects: small metal pieces and/or stones”
Where it was sold
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
Recall began
, by the company
FDA classified it
First in an FDA Enforcement Report
FDA event number
95916

The product recalled

As the FDA describes them, with the codes that tell whether a package is part of the recall.

  • F-0316-2025 Class II

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

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

    Quantity: 142 units

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Source and notes

U.S. Food and Drug Administration, Enforcement Reports (openFDA food recall data) (Public domain (U.S. government work); source U.S. Food and Drug Administration, openFDA), data as of January 1, 2025.

Each week the FDA lists the recalls it has classified in its Enforcement Report, often weeks after the company announced the recall, so a month with five weekly reports tends to count more. Each recall counts once, however many products it covers, in the month FDA first listed it. Class I means the food could cause serious harm or death, Class II temporary or minor harm, and Class III is unlikely to harm anyone. Meat, poultry and most egg products are recalled by the U.S. Department of Agriculture, not the FDA, and aren't included. For what to do with a recalled product, see the FDA's recalls page.