Food Recall Check
Class II · Moderate risk Terminated Initiated May 27, 2015 (11 years ago)

Glucosamine 750 mg recall

Recalled by Novacare, LLC · Murray, UT, United States

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

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

For someone with a food allergy the label is the only protection. An undeclared allergen can trigger a severe reaction even in a trace amount, which is why most of these recalls are Class I. All undeclared allergens recalls.

What was recalled

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

Quantity: 961 bottles.

Food: Dietary supplements

Lot codes, dates and UPCs

A recall covers only these codes. Compare them with the lot number, best-by date or UPC printed on your package.

Lot #s: 4102801, 2071918.2, 2061401, 2032006

Where it was sold

Nationwide.

Virginia

FDA's distribution note: Nationwide. No foreign or VA/govt/military consignees.

Check the codes, then return or discard. Class II means eating it may cause temporary or reversible health problems. If your package matches the recalled codes, do not eat it - return it to the store or throw it away. FDA lists this recall as terminated: the company has finished removing the product, so it should no longer be on shelves - but it can still be in a freezer or pantry.

Recalling firm
Novacare, LLC
Initiated by
Voluntary: Firm initiated
Recall initiated
May 27, 2015
In FDA report of
Aug 19, 2015
Terminated
Mar 27, 2017
FDA recall number
F-2946-2015 · event 71664
Official record
FDA enforcement report search

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