CLASS III Food recall · Reported 7 Feb 2024 · FDA Enforcement Report

Solgar, Triple Strength, Shellfish -Free recalled

Nestle Product Technology Center - Nestle Health Science is recalling Solgar, Triple Strength, Shellfish -Free, Glucosamine Chondroitin MSM per, distributed in Indiana, Nevada, New York, Pennsylvania, Tennessee, Texas. The recall was initiated on 22 Dec 2023 and the FDA has classified it as Class III.

Check your package

Lot, batch or date codesLot/Unit Numbers: 3250UM0704 UPC Codes: 041260351211
Quantity recalled612 bottles

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

Recall details

Recall number
F-0803-2024
FDA event ID
93707
Brand
Solgar
Classification
Class III
Status
Terminated
Recall initiated
22 Dec 2023
FDA classified
26 Jan 2024
Reported
7 Feb 2024
Type
Voluntary: Firm initiated
Customers notified by
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Reason category
Foreign Material
Product category
Oysters & Shellfish

Timeline

22 Dec 2023Recall initiated by company
26 Jan 2024Classified by FDA+35 days
7 Feb 2024Published in enforcement report+12 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

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.

Foreign material recalls cover pieces of metal, plastic, glass, wood or other objects that got into the product during processing and could cause injury if eaten.

Product as listed by the FDA

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

Where it was distributed

The recalled product was distributed to the following states: NY, IN, PA, TX, TN, NV

IndianaNevadaNew YorkPennsylvaniaTennesseeTexas

Questions about this recall

Why was it 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.

Which lots are affected?

Lot/Unit Numbers: 3250UM0704 UPC Codes: 041260351211

Where was it sold?

The recalled product was distributed to the following states: NY, IN, PA, TX, TN, NV

What should I do if I have it?

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

What does Class III mean?

Class III recalls are for products unlikely to cause any adverse health consequence, usually labelling or quality issues.

Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

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