Food Recall Check
Class II · Moderate risk Terminated Initiated Jan 9, 2020 (7 years ago)

Meijer Joint Health Movement Advanced Dietary Supplement with Glucosamine + Chondroitin recall

Recalled by Merical, LLC · Orange, CA, United States

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

Why it was recalled

Product label does not contain Crustacean Shellfish on the ingredient list or allergen information

Undeclared allergen: Shellfish

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

Meijer Joint Health Movement Advanced Dietary Supplement with Glucosamine + Chondroitin. 1500 mg; Supports Joint Mobility and Comfort; Unit Size - 80 count - 2 tablets per day. Item Numbers: MEIJER7383 UPC Code: 713733562966 Distributed by Meijer Distribution Inc. Grand Rapids, MI

Quantity: 977 cases

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.

Meijer Product Packaging Lot Number / Merical Batch Numbers; 812923955/300-00023955 817223961/300-00023961 833727345/300-00027345 908727346/300-00027346 916828561/300-00028561 918929999/300-00029999 924630013/300-00030013 928830746/300-00030746 935331728/300-00031728 Expiration dates: 04/01/2020, 06/01/2020, 08/01/2020, 03/01/2021,05/01/2021, 06/01/2021, 08/01/2021, 09/01/2021, 12/01/2021

Where it was sold

Michigan

FDA's distribution note: one customer , corporate in MI.

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. The risk from an undeclared allergen is to people allergic to shellfish; for anyone else the product is generally not a safety concern. 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
Merical, LLC
Initiated by
Voluntary: Firm initiated
Recall initiated
Jan 9, 2020
In FDA report of
Feb 12, 2020
Terminated
Aug 14, 2020
FDA recall number
F-0632-2020 · event 84690
Official record
FDA enforcement report search

Also recalled with it (1 more product)

FDA files each product of one recall action separately; these share the same FDA event.

Other recalls by Merical, LLC

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