Recall Radar

Nestle Product Technology Center - Nestle Health Science recalls Solgar: foreign object

February 7, 2024 · Nestle Product Technology Center - Nestle Health Science Class III

Class IIIFDA’s lowest-risk class: use of the product is not likely to cause adverse health consequences.
Reason for the recallNestle 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.

Find the official FDA enforcement report

Recall at a glance

Recalling company
Nestle Product Technology Center - Nestle Health Science
Location
Bridgewater, NJ
Reported by FDA
February 7, 2024
Recall started
December 22, 2023
Risk class
Class III
Status (latest data we have)
Terminated
Type
Voluntary: Firm initiated
Category
Supplements and infant formula
Reason type
Foreign materialLabeling and quality

Is my product affected?

Compare your product’s name, size and lot or date codes with the list below. A recall usually covers only specific codes.

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

Where it was distributed

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

What to do

If you have this product, check the codes above. FDA recall notices often tell consumers to stop eating the product and to return it or throw it away. Follow the company’s instructions and the official FDA information, and if you are unsure, do not eat it. If someone becomes ill after eating a recalled food, contact a healthcare professional. See FDA’s recalls and safety alerts for company announcements.

Frequently asked questions

What was recalled?

Nestle Product Technology Center - Nestle Health Science recalled 1 product, including Solgar, Triple Strength, Shellfish -Free, Glucosamine Chondroitin MSM, 120 Tablets per bottle. Glass Bottle, 12 per Case, Store at room….

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.

What does Class III mean?

FDA’s lowest-risk class: use of the product is not likely to cause adverse health consequences.

Where was it sold or shipped?

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

What should I do if I have this product?

Compare the product name, size and lot or date codes with the details on this page. FDA recall notices often tell you to stop eating the product and to return it or throw it away. Follow the company’s instructions and the official FDA information. If you are unsure, do not eat it.

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Sources

Data provided by the U.S. Food and Drug Administration (FDA) through openFDA, shown as published and not validated by this site. This site is independent and is not affiliated with or endorsed by FDA. It covers FDA-regulated foods; meat, poultry and egg products are regulated by USDA. Do not rely on this site for medical decisions: for health concerns contact a healthcare professional, and always follow the official notice and the company’s instructions. Terms and disclaimer.