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

Meijer Joint Health Triple Strength Formula Glucosamine recalled

Merical is recalling Meijer Joint Health Triple Strength Formula Glucosamine Hydrochloride 1500 mg, 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; 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

Quantity recalled2596 Packaged 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-0631-2020
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 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

Where it was distributed

one customer , corporate in MI.

Michigan

Stores named: Meijer

Questions about this recall

Is Meijer Joint Health Triple Strength Formula Glucosamine Hydrochloride 1500 mg recalled?

Yes. Merical recalled Meijer Joint Health Triple Strength Formula Glucosamine Hydrochloride 1500 mg on 9 Jan 2020. The recall is Class II and its status is Terminated. Recall number F-0631-2020.

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

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