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RECALL RECORD — CLASS IIIRecall closedF-0803-2024/FDA enforcement
Nestle Product Technology Center - Nestle Health Science·Food·Dec 22, 2023

Solgar, Triple Strength, Shellfish -Free, Glucosamine Chondroitin Msm, 120 Tablets Per Bottle

What you need to know

Class III

  • What happened

    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…

  • Health risk

    The product is unlikely to cause adverse health consequences. These recalls are often related to labeling or quality violations. A safety issue that does not fit the standard pathogen, allergen, chemical or quality categories.

  • Action required

    Check the identifying codes below and stop using the product. Return it to the retailer for a refund or dispose of it safely, following the recall notice.

Recall closed · classified by the FDANY, IN, PA, TX +2 moreMore food

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Match before you discard

Product identification

Source: FDA FOOD

Brand nameNestle Product Technology Center - Nestle Health Science
Recalling firmNestle Product Technology Center - Nestle Health ScienceBridgewater, NJ, United States
UPC / barcodes
0 41260 35121 1
Lot / date codes
  • Lot/Unit Numbers: 3250UM0704 UPC Codes: 041260351211
Distribution area
NYINPATXTNNV

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

United States

Quantity affected612 bottles
Recall initiationFDA report date: February 7, 2024
FDA recall numberF-0803-2024

Beyond the headline

The recall, in context

Nestle Product Technology Center - Nestle Health Science initiated this food recall on December 22, 2023. The FDA enforcement report states: 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. The FDA report lists distribution as: The recalled product was distributed to the following states: NY, IN, PA, TX, TN, NV.

The FDA enforcement report describes the reason as: 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.

Solgar, Triple Strength, Shellfish -Free, Glucosamine Chondroitin Msm, 120 Tablets Per Bottle was made or distributed by Nestle Product Technology Center - Nestle Health Science in Bridgewater, NJ, United States. This page reflects FDA report F-0803-2024, dated February 7, 2024.

Why this is a Class III recall

Class III means the product is unlikely to cause adverse health consequences. These recalls are often related to labeling or quality violations. In this recall, a safety issue that does not fit the standard pathogen, allergen, chemical or quality categories.

FDA definition

The product is unlikely to cause adverse health consequences. These recalls are often related to labeling or quality violations.

What to do now

  1. 1

    Stop using it

    Do not eat, drink or take the affected product.

  2. 2

    Check the codes

    Compare the UPC and lot code against the table above.

  3. 3

    Return or discard

    Contact the retailer or recalling firm about a refund, and dispose of the product safely.

Consumer safety guide

Product safety recall

Symptoms to watch for

The official enforcement report describes the specific risk. Follow the recall notice, check the product codes and do not use a product that may be affected.

Higher-risk groups

Children, pregnant people, older adults and people with weakened immune systems should take extra care when a product's safety is uncertain.

What to do now

  1. 1Stop using or eating the product and keep it away from children and pets.
  2. 2Check the UPC and lot/date codes on this page and follow the official recall notice for disposal or return.
  3. 3Seek medical advice if anyone develops severe or worrying symptoms after exposure.

Read the official source record for the specific hazard and instructions.

This is general consumer safety information, not medical advice or a diagnosis. Follow the official recall notice and contact a healthcare professional if you have concerns about exposure or symptoms.

Frequently asked

Questions about this recall

What is the Solgar, Triple Strength, Shellfish -Free, Glucosamine Chondroitin Msm, 120 Tablets Per Bottle recall?

Nestle Product Technology Center - Nestle Health Science recalled Solgar, Triple Strength, Shellfish -Free, Glucosamine Chondroitin Msm, 120 Tablets Per Bottle in an FDA Class III enforcement action reported as F-0803-2024. 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…

What should I do if I bought this product?

Check the identifying codes below and stop using the product. Return it to the retailer for a refund or dispose of it safely, following the recall notice. Stop using or eating the product and keep it away from children and pets. Check the UPC and lot/date codes on this page and follow the official recall notice for disposal or return. Seek medical advice if anyone develops severe or worrying symptoms after exposure.

Is the Nestle Product Technology Center - Nestle Health Science recall still active?

The FDA lists this recall as recall closed. It remains relevant if you still have the affected product or need to identify a historical recall.

Where can I verify this recall?

This page is normalized from the openFDA enforcement record F-0803-2024. You can verify it directly using the official source link on this page. VerifyRecall updates its index from public FDA enforcement data and does not replace advice from the FDA, the recalling firm or a healthcare professional.

Verify before you act.

VerifyRecall is independent and not affiliated with the FDA. Always confirm the latest status on the official source record.

Official source

Brand history

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Record last synced from official openFDA enforcement data on November 14, 2026. Source record: official FDA notice.