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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

Solgar Glucosamine Chondroitin MSM Recalled for Mislabeled Contents

Agency Publication Date: January 26, 2024
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Summary

Nestle Health Science is recalling 612 bottles of Solgar Triple Strength Shellfish-Free Glucosamine Chondroitin MSM dietary supplements. This recall was issued because the bottles were incorrectly filled with Megasorb B-Complex tablets instead of the intended Glucosamine and Chondroitin supplement. No incidents or injuries have been reported to date.

Risk

Consumers taking the mislabeled product will be consuming B-complex vitamins instead of the intended joint health supplement. While the health risk is considered low, the product does not contain the ingredients listed on the label, and consumers may unknowingly ingest high doses of B vitamins.

What You Should Do

  1. This recall affects 120-tablet glass bottles of Solgar Triple Strength Shellfish-Free Glucosamine Chondroitin MSM (Product Number 1319) with lot number 3250UM0704 and UPC 041260351211.
  2. Return the product to the place of purchase for a refund, throw it away, or contact Nestle Health Science for further instructions.
  3. Call the FDA Consumer Complaint hotline at 1-888-723-3332 or visit www.fda.gov/safety/recalls 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: Solgar Triple Strength Shellfish-Free Glucosamine Chondroitin MSM (120 Tablets)
Variants: Triple Strength, Shellfish-Free, 120 Tablets
Item Code:
1319
UPC Codes:
041260351211
Lot Numbers:
3250UM0704

Bottles were incorrectly filled with Megasorb B-Complex product instead of the labeled supplement contents.

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 93707
Status: Resolved
Manufacturer: Nestle Product Technology Center - Nestle Health Science
Manufactured In: United States
Units Affected: 612 bottles
Distributed To: New York, Indiana, Pennsylvania, Texas, Tennessee, Nevada

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.