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RECALL RECORD — CLASS IIRecall closedF-0316-2025/FDA enforcement
Zoe US, INC.·Dietary Supplements·Dec 4, 2024

Zoe Brand Daily 30+ Prebiotic Blend

What you need to know

Class II

  • What happened

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

  • Health risk

    The product may cause temporary or medically reversible health consequences, or the probability of serious harm is remote. Metal fragments can cause cuts, choking or internal injury if swallowed.

  • Action required

    Stop taking the supplement. Check the lot and UPC codes below, then return it to the retailer or contact the manufacturer about a refund. Seek medical advice if you have concerns about exposure.

Recall closed · classified by the FDADistribution not listedMore supplements

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Product identification

Source: FDA FOOD

Brand nameZoe US, INC.
Recalling firmZoe US, INC.Canton, MA, United States
UPC / barcodesNo UPC listed in the FDA enforcement record.
Lot / date codes
  • Expiration Date: 10/31/25 batch numbers: 24269, 24287, 24288
Distribution area

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

Mexico

Quantity affected142 units
Recall initiationFDA report date: January 1, 2025
FDA recall numberF-0316-2025

Beyond the headline

The recall, in context

Zoe US, INC. initiated this supplements recall on December 4, 2024. The FDA enforcement report states: Product may contain foreign objects: small metal pieces and/or stones. The FDA report lists distribution as: 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.

The FDA enforcement report describes the reason as: Product may contain foreign objects: small metal pieces and/or stones

Zoe Brand Daily 30+ Prebiotic Blend was made or distributed by Zoe US, INC. in Canton, MA, United States. This page reflects FDA report F-0316-2025, dated January 1, 2025.

Why this is a Class II recall

Class II means the product may cause temporary or medically reversible health consequences, or the probability of serious harm is remote. In this recall, metal fragments can cause cuts, choking or internal injury if swallowed.

FDA definition

The product may cause temporary or medically reversible health consequences, or the probability of serious harm is remote.

What to do now

  1. 1

    Stop using it

    Do not eat, drink or take the affected product.

  2. 2

    Check the codes

    Compare the lot and date codes against the table above.

  3. 3

    Return or discard

    Contact the retailer or recalling firm about a refund, and dispose of the product safely.

Consumer safety guide

Metal contamination

Possible health effects

Metal fragments can cause cuts, choking or internal injury. Do not inspect or taste a suspect product.

Higher-risk groups

Children, older adults and anyone who may swallow a fragment without noticing are at greater risk.

What to do now

  1. 1Stop eating or using the product; do not try to find the fragment by tasting or chewing.
  2. 2Seek medical care if anyone has swallowed metal or has severe throat, chest or abdominal pain.
  3. 3Keep the packaging and contact the retailer or manufacturer about a refund.

This is general consumer safety information, not medical advice or a diagnosis. Follow the official recall notice and contact a healthcare professional if you have concerns about exposure or symptoms.

Frequently asked

Questions about this recall

What is the Zoe Brand Daily 30+ Prebiotic Blend recall?

Zoe US, INC. recalled Zoe Brand Daily 30+ Prebiotic Blend in an FDA Class II enforcement action reported as F-0316-2025. Product may contain foreign objects: small metal pieces and/or stones

What should I do if I bought this product?

Stop taking the supplement. Check the lot and UPC codes below, then return it to the retailer or contact the manufacturer about a refund. Seek medical advice if you have concerns about exposure. Stop eating or using the product; do not try to find the fragment by tasting or chewing. Seek medical care if anyone has swallowed metal or has severe throat, chest or abdominal pain. Keep the packaging and contact the retailer or manufacturer about a refund.

Is the Zoe US, INC. recall still active?

The FDA lists this recall as recall closed. It remains relevant if you still have the affected product or need to identify a historical recall.

Where can I verify this recall?

This page is normalized from the openFDA enforcement record F-0316-2025. You can verify it directly using the official source link on this page. VerifyRecall updates its index from public FDA enforcement data and does not replace advice from the FDA, the recalling firm or a healthcare professional.

Verify before you act.

VerifyRecall is independent and not affiliated with the FDA. Always confirm the latest status on the official source record.

Official source

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Record last synced from official openFDA enforcement data on November 14, 2026. Source record: official FDA notice.