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Recall data is sourced from official U.S. government agencies (CPSC, FDA, NHTSA, USDA) and processed using AI to improve readability. This site is not affiliated with or endorsed by any government agency. Always refer to the original agency notice for authoritative information.

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Medium RiskFDA Food
Food & Beverages/Dietary Supplements

Church & Dwight Co., Inc. OGI Distribution Center: vitafusion Gummy Supplements Recalled for Potential Metal Mesh Contamination

Agency Publication Date: April 28, 2021
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Summary

Approximately 18,308 bottles of various vitafusion gummy supplements, including MultiVites, Fiber Well, Melatonin, Kids Melatonin, and SleepWell, are being recalled due to the potential presence of metallic mesh material. This issue was identified after the firm initiated a voluntary recall following reports of foreign material. Consumers should check their supplement bottles for specific lot codes to see if their product is affected. Church & Dwight is advising anyone who has these products to stop using them and return them for a refund.

Risk

The ingestion of metallic mesh material can cause serious injury, including damage to the digestive tract or choking. The firm has initiated this recall to prevent potential harm from these physical contaminants.

What You Should Do

  1. Check your vitafusion supplement bottles for the following product names and lot codes: vitafusion MultiVites 150ct (Lot WA03044959), Fiber Well 220ct (Lots WA03087520, WA02487524, WA03086273), Fiber Well 90ct (Lots WA02187020, WA03086671, WA03087521), Melatonin 140ct or 44ct (Lots WA03076990, WA03077852, WA02608988, WA03076270), Kids Melatonin 50ct (Lot WA03076268), or SleepWell 250ct (Lot WA03077414).
  2. Verify the UPC/Product Codes on your bottle: 027917019192, 027917019840, 027917018904, 0-27917-02671-8, 0-27917-28011-0, 027917001708, or 0-27917-02524-7.
  3. Stop using the recalled supplements immediately to avoid the risk of ingesting foreign metal material.
  4. Return the affected product to the place of purchase for a full refund or contact the manufacturer, Church & Dwight Co., Inc., for further instructions regarding the disposal or return of the supplements.
  5. If you have consumed these products and feel unwell, contact your healthcare provider immediately.
  6. For additional questions, contact the FDA Consumer Complaint hotline at 1-888-723-3332 (1-888-SAFEFDA).

Your Remedy Options

💰Full Refund

Return to the place of purchase for a full refund or contact the manufacturer for further instructions

How to: Consumers should return the recalled supplements to the retailer where they were purchased to receive a refund.

Affected Products

Product: vitafusion MultiVites (150ct)
UPC Codes:
027917019192
Lot Numbers:
WA03044959
Product: vitafusion Fiber Well (220ct)
Item Code:
10 / 220 CT
UPC Codes:
027917019840
Lot Numbers:
WA03087520
WA02487524
WA03086273
Product: vitafusion Fiber Well (90ct)
Item Code:
4/3 Pack 90CT
UPC Codes:
027917018904
Lot Numbers:
WA02187020
WA03086671
WA03087521
Product: vitafusion Melatonin (140ct and 44ct)
Item Code:
3 Pack 140 CT
3 Pack 44CT
UPC Codes:
027917026718
027917280110
Lot Numbers:
WA03076990
WA03077852
WA02608988
WA03076270
Product: vitafusion Kids Melatonin (50ct)
Item Code:
4 / 3 PACK 50CT
UPC Codes:
027917001708
Lot Numbers:
WA03076268
Product: vitafusion SleepWell (250ct)
Item Code:
24 / 250 CT
UPC Codes:
027917025247
Lot Numbers:
WA03077414

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 87745
Status: Resolved
Manufacturer: Church & Dwight Co., Inc. OGI Distribution Center
Manufactured In: United States
Units Affected: 6 products (683 Bottles; 2928 Bottles; 7782 Bottles; 5475 Bottles 44ct Bottles, 2081 Bottles 140 CT; 1320 Bottles; 120 Bottles)
Distributed To: Nationwide

Were You Affected by This Recall?

If you or a family member were harmed by this recalled product, you may have legal rights. Consider consulting a consumer protection attorney to understand your options for compensation.

Find an Attorney

This is general information, not legal advice. Go Backs is not a law firm and does not provide legal services.

AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.

Sources: FDA iRES · Raw API Response

openFDA Disclaimer: This recall information is sourced from the openFDA API. Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Refer to the openFDA terms of service for more information.