RecallHawk
Class III Recall

Solgar, Triple Strength, Shellfish -Free, Glucosamine Chondroitin MSM, 120 Tablets per bottle. Glass Bottle, 12 per Cas

Nestle Product Technology Center - Nestle Health Science

Summary

The FDA issued a Class III for Solgar, Triple Strength, Shellfish -Free, Glucosamine Chondroitin MSM, 120 Tabl by Nestle Product Technology Center - Nestle Health Science. Reason: Nestle Health Science has initiated a recall of Solgar Glucosamine Chondroitin, 120 Tablets, in Glass bottle, 12 bottles per case because of error dur.

Details

Source

Food Recall

External ID

F-0803-2024

Action Date

2024-02-07

Status

Terminated

Category

food

Product Description

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

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

Quantity Affected: 612 bottles

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.

Distribution

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

Type: Voluntary: Firm initiated

Recall Initiated: 2023-12-22

Context & Analysis

This is a Class III recall. Class III recalls involve products unlikely to cause adverse health consequences, but that violate FDA regulations.

This was one of 56 food recalls issued in the same week, part of 204 food-related FDA actions this month.

Nestle Product Technology Center - Nestle Health Science has 2 FDA actions in our database, including 2 recalls.

Frequently Asked Questions

What is a Class III recall?

A Class III recall involves products that are unlikely to cause adverse health effects but violate FDA labeling or manufacturing regulations.

What should I do if I have this product?

Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (Nestle Product Technology Center - Nestle Health Science) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Nestle Product Technology Center - Nestle Health Science have FDA actions?

Nestle Product Technology Center - Nestle Health Science has 2 FDA actions in our database, including 2 recalls and 0 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "F-0803-2024" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

Want to know the moment something like this happens?

Get alerts for food

Related Actions