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