Food Recall Check
Class III · Low risk Terminated Initiated Dec 22, 2023 (3 years ago)

Solgar Triple Strength recall

Recalled by Nestle Product Technology Center - Nestle Health Science · Bridgewater, NJ, United States

Class III — Low risk. Unlikely to cause harm, but violates FDA regulations.

Why it was recalled

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.

Hard or sharp fragments can cut the mouth or throat, break teeth or cause choking. They usually come from equipment wear or packaging on the production line. All foreign material recalls.

What was recalled

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

Quantity: 612 bottles

Food: Dietary supplements

Lot codes, dates and UPCs

A recall covers only these codes. Compare them with the lot number, best-by date or UPC printed on your package.

Lot/Unit Numbers: 3250UM0704 UPC Codes: 041260351211

Where it was sold

Indiana Nevada New York Pennsylvania Tennessee Texas

FDA's distribution note: The recalled product was distributed to the following states: NY, IN, PA, TX, TN, NV

Low risk, but check. Class III means the product is unlikely to make anyone ill but breaks an FDA rule, often a labeling one. If your package matches, the store will normally refund it. FDA lists this recall as terminated: the company has finished removing the product, so it should no longer be on shelves - but it can still be in a freezer or pantry.

Recalling firm
Nestle Product Technology Center - Nestle Health Science
Initiated by
Voluntary: Firm initiated
Recall initiated
Dec 22, 2023
In FDA report of
Feb 7, 2024
Terminated
Mar 26, 2024
FDA recall number
F-0803-2024 · event 93707
Official record
FDA enforcement report search

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