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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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Low RiskFDA Food
Food & Beverages/Dietary Supplements

GNC Women's 30+ Vitapak Recalled for Undeclared Fish Allergen

Agency Publication Date: June 5, 2025
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Summary

GNC Holdings LLC is recalling 144,430 units of GNC Women's 30+ Vitapak dietary supplements because they contain an undeclared fish allergen (parvalbumin). The product is sold in paper-board cartons containing 30 individual sachets, each holding four tablets and a capsule. No injuries or illnesses have been reported to date, but the supplement could be dangerous to those with specific allergies. Consumers should return the product to GNC for a refund or dispose of it.

Risk

The product contains fish which is not listed on the label. People with an allergy or severe sensitivity to fish (parvalbumin) risk a serious or life-threatening allergic reaction if they consume this product.

What You Should Do

  1. This recall affects GNC Women's 30+ Vitapak cartons containing 30 sachets with lot numbers 1060EB2401, 1060EB2402, 1060EB2403, 1060EB2404, 1060EB2405, 1060EB2501, 1060EB2502, and 1060EB2503.
  2. Check the lot number printed on your carton to determine if your product is part of this recall.
  3. Return the product to the place of purchase for a refund, throw it away, or contact the manufacturer for further instructions.
  4. Call the FDA Consumer Complaint hotline at 1-888-723-3332 (1-888-SAFEFDA) for additional questions.

Your Remedy Options

You have 2 options:

๐Ÿ’ฐOption 1: Full Refund
How to: Return the product to the place of purchase for a full refund, or contact the manufacturer or supplier for further instructions
๐Ÿ—‘๏ธOption 2: Dispose of Product
How to: Throw the product away.

Affected Products

Product: GNC Women's 30+ Vitapak (30 Sachets)
Lot Numbers:
1060EB2401
1060EB2402
1060EB2403
1060EB2404
1060EB2405
1060EB2501
1060EB2502
1060EB2503

Paper-board carton (10.25" x 3.56" x 3.15") containing 30 sachets with tear notches. Recall number F-0928-2025.

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 96759
Status: Resolved
Manufacturer: GNC Holdings LLC
Sold By: GNC
Manufactured In: United States
Units Affected: 144,430 Units
Distributed To: Alabama, Arkansas, Arizona, California, Colorado, Connecticut, District of Columbia, Delaware, Florida, Georgia, Hawaii, Iowa, Idaho, Illinois, Indiana, Kansas, Kentucky, Louisiana, Massachusetts, Maryland, Maine, Michigan, Minnesota, Missouri, Mississippi, North Carolina, North Dakota, Nebraska, New Hampshire, New Jersey, New Mexico, Nevada, New York, Ohio, Oklahoma, Oregon, Pennsylvania, Puerto Rico, Rhode Island, South Carolina, Tennessee, Texas, Utah, Virginia, Washington, Wisconsin, West Virginia, Wyoming

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 ยท 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.