CLASS II Food recall · Reported 12 Feb 2020 · FDA Enforcement Report

Meijer Joint Health Movement Advanced Dietary Supplement recalled

Merical is recalling Meijer Joint Health Movement Advanced Dietary Supplement with Glucosamine + Chondroitin, distributed in Michigan. The recall was initiated on 9 Jan 2020 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesMeijer 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

Quantity recalled977 cases

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

Recall details

Recall number: F-0632-2020
FDA event ID: 84690
Recalling firm: Merical, Orange, CA
Brand: Meijer Joint
Classification: Class II
Status: Terminated
Recall initiated: 9 Jan 2020
FDA classified: 4 Feb 2020
Reported: 12 Feb 2020
Type: Voluntary: Firm initiated
Customers notified by: Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Reason category: Undeclared Allergens
Product category: Fish

Timeline

9 Jan 2020	Recall initiated by company
4 Feb 2020	Classified by FDA	+26 days
12 Feb 2020	Published in enforcement report	+8 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

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

Food allergen labelling is required by US law for the nine major allergens. A product recalled for an undeclared allergen is only a risk to people with that allergy; everyone else can consume it safely.

Product as listed by the FDA

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

Where it was distributed

one customer , corporate in MI.

Michigan

Stores named: Meijer

Questions about this recall

Why was it recalled?

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

Which lots are affected?

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 was it sold?

one customer , corporate in MI.

What should I do if I have it?

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

What does Class II mean?

Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.

Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

Other products in this recall event

1 other product · FDA event 84690

This product is part of a recall event; the main page for the event is Meijer Joint Health Triple Strength Formula Glucosamine recalled.

Reported	Class	Recall	Company	Reason	Where
12 Feb 2020	CLASS II	Meijer Joint Health Triple Strength Formula Glucosamine recalledMeijer Joint	Merical	Undeclared Allergens	MI

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