CLASS II Food recall · Reported 1 Jan 2025 · FDA Enforcement Report

ZOE Daily 30+ Prebiotic blend recalled by Zoe US

Zoe US is recalling ZOE Daily 30+ Prebiotic blend, distributed in 26 states. The recall was initiated on 4 Dec 2024 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesExpiration Date: 10/31/25 batch numbers: 24269, 24287, 24288
Quantity recalled142 units

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

Recall details

Recall number
F-0316-2025
FDA event ID
95916
Recalling firm
Zoe US, Canton, MA
Brand
Zoe
Classification
Class II
Status
Terminated
Recall initiated
4 Dec 2024
FDA classified
24 Dec 2024
Reported
1 Jan 2025
Type
Voluntary: Firm initiated
Customers notified by
E-Mail
Reason category
Foreign Material
Product category
Probiotics

Timeline

4 Dec 2024Recall initiated by company
24 Dec 2024Classified by FDA+20 days
1 Jan 2025Published in enforcement report+8 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

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

Foreign material recalls cover pieces of metal, plastic, glass, wood or other objects that got into the product during processing and could cause injury if eaten.

Product as listed by the FDA

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

Where it was distributed

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

ArizonaCaliforniaColoradoConnecticutDistrict of ColumbiaFloridaGeorgiaHawaiiIllinoisKentuckyMassachusettsMaineMichiganMinnesotaNorth CarolinaNew JerseyNew MexicoNew YorkPennsylvaniaSouth Carolina

Questions about this recall

Why was it recalled?

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

Which lots are affected?

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

Where was it 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

What should I do if I have it?

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

What does Class II mean?

Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.

Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

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