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Class II: temporary or reversible health riskTerminated

Novacare Glucosamine 750 mg 120 ct Recall

Glucosamine 750 mg 120 ct, Capsule, Dosage: 12 capsules, 750 mg ea

Novacare, LLC · Murray, UT

Risk level
Class II
Reported by FDA
Aug 19, 2015
Recall ID
F-2946-2015
Check your lot numberHow we source this data

Summary

Novacare recalled Glucosamine 750 mg 120 ct starting May 27, 2015. The FDA classified it as Class II (temporary or reversible health risk) and published enforcement report F-2946-2015 on Aug 19, 2015. Reason: TSN Labs is conducting a field action on Glucosamine 750 mg 120 ct due to inadequate allergen labeling. Status: Terminated.

Why it was recalled

TSN Labs is conducting a field action on Glucosamine 750 mg 120 ct due to inadequate allergen labeling.

Product description

Glucosamine 750 mg 120 ct, Capsule, Dosage: 12 capsules, 750 mg ea., three times daily with meals

Lot numbers, UPCs & expiration codes

Lot #s: 4102801, 2071918.2, 2061401, 2032006

Where it was sold

Nationwide. No foreign or VA/govt/military consignees.

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-2946-2015
Classification
Class II
Status
Terminated
Recall initiated
May 27, 2015
FDA report date
Aug 19, 2015
Quantity
961 bottles.
Recall type
Voluntary: Firm initiated
Recalling firm
Novacare, LLC

Original FDA data

Every field from FDA enforcement report F-2946-2015, exactly as published.

Show all FDA fields
City
Murray
State
UT
Status
Terminated
Country
United States
Event ID
71664
Address
312 W 6100 S
Code information
Lot #s: 4102801, 2071918.2, 2061401, 2032006
Postal code
84107-6990
Report date
Aug 19, 2015
Product type
Food
Recall number
F-2946-2015
Classification
Class II
Recalling firm
Novacare, LLC
Product quantity
961 bottles.
Termination date
Mar 27, 2017
Reason for recall
TSN Labs is conducting a field action on Glucosamine 750 mg 120 ct due to inadequate allergen labeling.
Voluntary / mandated
Voluntary: Firm initiated
Product description
Glucosamine 750 mg 120 ct, Capsule, Dosage: 12 capsules, 750 mg ea., three times daily with meals
Distribution pattern
Nationwide. No foreign or VA/govt/military consignees.
Recall initiation date
May 27, 2015
Initial firm notification
Letter
Center classification date
Aug 11, 2015

How we source this data

Source: U.S. Food and Drug Administration enforcement report F-2946-2015, published Aug 19, 2015. View the source record (openFDA) · FDA enforcement reports

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

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