Food recall

Nestle Product Technology Center - Nestle Health Science recall: Solgar, Triple Strength, Shellfish -Free, Glucosamine Chondroitin MSM

Nestle Product Technology Center - Nestle Health Science, of Bridgewater, NJ, recalled Solgar, Triple Strength, Shellfish -Free, Glucosamine Chondroitin MSM. The FDA's reason: “Nestle Health Science has initiated a recall of Solgar Glucosamine Chondroitin, 120 Tablets, in Glass bottle, 12 bottles per case because of error during packaging in which a A Megasorb B-Complex...” The FDA classified it Class III: it is unlikely to cause harm. The company began the recall voluntarily on December 22, 2023, and the FDA first listed it in its Enforcement Report of February 7, 2024. The FDA has closed the recall: it found the company did all it reasonably could to remove or correct the product.

How serious

Class III

It is unlikely to cause harm

Why

Metal, plastic, glass or other objects

Status

Terminated

Closed March 26, 2024

The recall

Company
Nestle Product Technology Center - Nestle Health Science (Bridgewater, NJ)
Reason, in FDA's words
“Nestle Health Science has initiated a recall of Solgar Glucosamine Chondroitin, 120 Tablets, in Glass bottle, 12 bottles per case because of error during packaging in which a A Megasorb B-Complex product was filled into bottles labeled as Glucosamine_Chondroitin MSM.”
Where it was sold
The recalled product was distributed to the following states: NY, IN, PA, TX, TN, NV
Recall began
, by the company
FDA classified it
First in an FDA Enforcement Report
FDA event number
93707

The product recalled

As the FDA describes them, with the codes that tell whether a package is part of the recall.

  • F-0803-2024 Class III

    Solgar, Triple Strength, Shellfish -Free, Glucosamine Chondroitin MSM, 120 Tablets per bottle. Glass Bottle, 12 per Case, Store at room temperature . Product Number -1319

    Codes: Lot/Unit Numbers: 3250UM0704 UPC Codes: 041260351211

    Quantity: 612 bottles

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Source and notes

U.S. Food and Drug Administration, Enforcement Reports (openFDA food recall data) (Public domain (U.S. government work); source U.S. Food and Drug Administration, openFDA), data as of February 7, 2024.

Each week the FDA lists the recalls it has classified in its Enforcement Report, often weeks after the company announced the recall, so a month with five weekly reports tends to count more. Each recall counts once, however many products it covers, in the month FDA first listed it. Class I means the food could cause serious harm or death, Class II temporary or minor harm, and Class III is unlikely to harm anyone. Meat, poultry and most egg products are recalled by the U.S. Department of Agriculture, not the FDA, and aren't included. For what to do with a recalled product, see the FDA's recalls page.