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RECALL RECORD — CLASS IIRecall closedF-1456-2014/FDA enforcement
Health Wright Products INC·Dietary Supplements·Oct 25, 2013

Glucosamine, Chondroitin, Msm Plus, Dietary Supplement, 60 Capsules Per Bottle

What you need to know

Class II

  • What happened

    Dietary supplement products are recalled because they were made from ingredient that was contaminated with Chloramphenicol.

  • Health risk

    The product may cause temporary or medically reversible health consequences, or the probability of serious harm is remote. A safety issue that does not fit the standard pathogen, allergen, chemical or quality categories.

  • Action required

    Stop taking the supplement. Check the lot and UPC codes below, then return it to the retailer or contact the manufacturer about a refund. Seek medical advice if you have concerns about exposure.

Recall closed · classified by the FDADistribution not listedMore supplements

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Product identification

Source: FDA FOOD

Brand nameHealth Wright Products INC
Recalling firmHealth Wright Products INCClackamas, OR, United States
UPC / barcodesNo UPC listed in the FDA enforcement record.
Lot / date codes
  • LOT# 1125804, EXP 09/14 (means September 2014)
  • LOT# 1214301, EXP 05/15 (means May 2015)
  • LOT# 1308601
  • EXP 03/16 (means March 2016)
Distribution area

Distributed to California, Florida, Oregon, Utah, and Mexico

Mexico

Quantity affected3127 bottles
Recall initiationFDA report date: February 5, 2014
FDA recall numberF-1456-2014

Beyond the headline

The recall, in context

Health Wright Products INC initiated this supplements recall on October 25, 2013. The FDA enforcement report states: Dietary supplement products are recalled because they were made from ingredient that was contaminated with Chloramphenicol. The FDA report lists distribution as: Distributed to California, Florida, Oregon, Utah, and Mexico.

The FDA enforcement report describes the reason as: Dietary supplement products are recalled because they were made from ingredient that was contaminated with Chloramphenicol.

Glucosamine, Chondroitin, Msm Plus, Dietary Supplement, 60 Capsules Per Bottle was made or distributed by Health Wright Products INC in Clackamas, OR, United States. This page reflects FDA report F-1456-2014, dated February 5, 2014.

Why this is a Class II recall

Class II means the product may cause temporary or medically reversible health consequences, or the probability of serious harm is remote. In this recall, a safety issue that does not fit the standard pathogen, allergen, chemical or quality categories.

FDA definition

The product may cause temporary or medically reversible health consequences, or the probability of serious harm is remote.

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 lot and date codes 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 Glucosamine, Chondroitin, Msm Plus, Dietary Supplement, 60 Capsules Per Bottle recall?

Health Wright Products INC recalled Glucosamine, Chondroitin, Msm Plus, Dietary Supplement, 60 Capsules Per Bottle in an FDA Class II enforcement action reported as F-1456-2014. Dietary supplement products are recalled because they were made from ingredient that was contaminated with Chloramphenicol.

What should I do if I bought this product?

Stop taking the supplement. Check the lot and UPC codes below, then return it to the retailer or contact the manufacturer about a refund. Seek medical advice if you have concerns about exposure. 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 Health Wright Products INC 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-1456-2014. 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

More recalls by Health Wright Products INC

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Class II·

Health Wright Products INC

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Dietary supplement products are recalled because they were made from ingredient that was contaminated with Chloramphenicol.

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Class II·

Health Wright Products INC

Digest Ultra, Dietary Supplement, Packaged 56 Capsules Per Bottle or Distributed in Bulk, Sold…

Dietary supplement products are recalled because they were made from ingredient that was contaminated with Chloramphenicol.

Distribution not listedSupplements

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