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Class III: unlikely to cause harmTerminated

Nestle Product Technology Center - Nestle Health Science Solgar Recall

Solgar, Triple Strength, Shellfish -Free, Glucosamine Chondroitin MSM, 120 Tablets per…

Nestle Product Technology Center - Nestle Health Science · Bridgewater, NJ

Risk level
Class III
Reported by FDA
Feb 7, 2024
Recall ID
F-0803-2024
Check your lot numberHow we source this data

Summary

Nestle Product Technology Center - Nestle Health Science recalled Solgar starting Dec 22, 2023. The FDA classified it as Class III (unlikely to cause harm) and published enforcement report F-0803-2024 on Feb 7, 2024. Reason: 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. Status: Terminated.

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.

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 numbers, UPCs & expiration codes

Lot/Unit Numbers: 3250UM0704 UPC Codes: 041260351211

Where it was sold

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

What to do if you have this product

  • Compare the brand, size, and lot/UPC codes on your package with the codes above.
  • If it matches, don't eat it. Return it to the store for a refund or throw it away.
  • Wash surfaces and containers that touched the product.
  • If you feel sick after eating it, contact your doctor. In an emergency call 911.

Recall details

Recall number
F-0803-2024
Classification
Class III
Status
Terminated
Recall initiated
Dec 22, 2023
FDA report date
Feb 7, 2024
Quantity
612 bottles
Recall type
Voluntary: Firm initiated
Recalling firm
Nestle Product Technology Center - Nestle Health Science

Original FDA data

Every field from FDA enforcement report F-0803-2024, exactly as published.

Show all FDA fields
City
Bridgewater
State
NJ
Status
Terminated
Country
United States
Event ID
93707
Address
1007 Us Highway 202/206 Bldg Jr2
Code information
Lot/Unit Numbers: 3250UM0704 UPC Codes: 041260351211
Postal code
08807-1275
Report date
Feb 7, 2024
Product type
Food
Recall number
F-0803-2024
Classification
Class III
Recalling firm
Nestle Product Technology Center - Nestle Health Science
Product quantity
612 bottles
Termination date
Mar 26, 2024
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.
Voluntary / mandated
Voluntary: Firm initiated
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
Distribution pattern
The recalled product was distributed to the following states: NY, IN, PA, TX, TN, NV
Recall initiation date
Dec 22, 2023
Initial firm notification
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Center classification date
Jan 26, 2024

How we source this data

Source: U.S. Food and Drug Administration enforcement report F-0803-2024, published Feb 7, 2024. View the source record (openFDA) · FDA enforcement reports

Last checked against FDA data: . Content last changed: .

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