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

Meijer Joint Health Triple Strength Formula Glucosamine Hydrochloride 1500 mg 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 Triple Strength Formula Glucosamine Hydrochloride 1500 mg; Helps Overall Joint Physical Function; Unit Size - 40 count and 80 count - 2 tablets per day. Item Numbers: MEIJER7754 (40 count) & MEIJER7755 (80 count) UPC Code: 713733563024 & 713733563031 respectively Distributed by Meijer Distribution Inc. Grand Rapids, MI

Quantity: 2596 Packaged Cases

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; 813623939 / 300-00023939 819223940 / 300-00023940 825326387 / 300-00026387 831125997 / 300-00025997 904327090 / 300-00027090 909228407 / 300-00028407 923129433 / 300-00029433 813623941 / 300-00023941 819223942 / 300-00023942 825025436 / 300-00025436 829726962 / 300-00026962 831126959 / 300-00026959 833327088 / 300-00027088 904327255 / 300-00027255 910128408 / 300-00028408 923930450 / 300-00030450 918229434 / 300-00029434 923130315 / 300-00030315 932930456 / 300-00030456 932531502 / 300-00031502 Expiration Dates: 04/01/2020, 06/01/2020, 08/01/2020, 10/01/2020, 02/01/2021, 03/01/2021, 06/01/2021, 08/01/2021, 10/01/2021, 11/01/2021

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-0631-2020 · 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