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RECALL RECORD — CLASS IIRecall closedF-0631-2020/FDA enforcement
Merical, LLC·Food·Jan 9, 2020

Meijer Joint Health Triple Strength Formula Glucosamine Hydrochloride 1500 mg

What you need to know

Class II

  • What happened

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

  • Health risk

    The product may cause temporary or medically reversible health consequences, or the probability of serious harm is remote. A safety issue that does not fit the standard pathogen, allergen, chemical or quality categories.

  • Action required

    Check the identifying codes below and stop using the product. Return it to the retailer for a refund or dispose of it safely, following the recall notice.

Recall closed · classified by the FDAIN, MIMore food

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Match before you discard

Product identification

Source: FDA FOOD

Brand nameMerical, LLC
Recalling firmMerical, LLCOrange, CA, United States
UPC / barcodes
7 13733 56302 47 13733 56303 1
Lot / date codes
  • 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
Distribution area
INMI

one customer, corporate in MI.

United States

Quantity affected2596 Packaged Cases
Recall initiationFDA report date: February 12, 2020
FDA recall numberF-0631-2020

Beyond the headline

The recall, in context

Merical, LLC initiated this food recall on January 9, 2020. The FDA enforcement report states: Product label does not contain Crustacean Shellfish on the ingredient list or allergen information. The FDA report lists distribution as: one customer , corporate in MI.

The FDA enforcement report describes the reason as: Product label does not contain Crustacean Shellfish on the ingredient list or allergen information

Meijer Joint Health Triple Strength Formula Glucosamine Hydrochloride 1500 mg was made or distributed by Merical, LLC in Orange, CA, United States. This page reflects FDA report F-0631-2020, dated February 12, 2020.

Why this is a Class II recall

Class II means the product may cause temporary or medically reversible health consequences, or the probability of serious harm is remote. In this recall, a safety issue that does not fit the standard pathogen, allergen, chemical or quality categories.

FDA definition

The product may cause temporary or medically reversible health consequences, or the probability of serious harm is remote.

What to do now

  1. 1

    Stop using it

    Do not eat, drink or take the affected product.

  2. 2

    Check the codes

    Compare the UPC and lot code against the table above.

  3. 3

    Return or discard

    Contact the retailer or recalling firm about a refund, and dispose of the product safely.

Consumer safety guide

Undeclared allergen

Symptoms to watch for

Hives, swelling, wheezing, coughing, vomiting, abdominal pain or a drop in blood pressure. Anaphylaxis is a medical emergency.

When symptoms may appear

Allergic reactions often begin within minutes to a few hours of eating the allergen.

Higher-risk groups

Anyone with a diagnosed food allergy, especially children, and people with a history of anaphylaxis or asthma.

What to do now

  1. 1Do not eat or serve the affected product if you or anyone in the household has a diagnosed allergy.
  2. 2If symptoms such as swelling, wheezing or breathing difficulty occur, use the person's prescribed emergency plan and call emergency services.
  3. 3Keep the packaging, contact the retailer or manufacturer for a refund, and read the official recall notice for the exact allergen.

For a severe allergic reaction, do not wait for a callback or refund process before seeking emergency care.

This is general consumer safety information, not medical advice or a diagnosis. Follow the official recall notice and contact a healthcare professional if you have concerns about exposure or symptoms.

Frequently asked

Questions about this recall

What is the Meijer Joint Health Triple Strength Formula Glucosamine Hydrochloride 1500 mg recall?

Merical, LLC recalled Meijer Joint Health Triple Strength Formula Glucosamine Hydrochloride 1500 mg in an FDA Class II enforcement action reported as F-0631-2020. Product label does not contain Crustacean Shellfish on the ingredient list or allergen information

What should I do if I bought this product?

Check the identifying codes below and stop using the product. Return it to the retailer for a refund or dispose of it safely, following the recall notice. Do not eat or serve the affected product if you or anyone in the household has a diagnosed allergy. If symptoms such as swelling, wheezing or breathing difficulty occur, use the person's prescribed emergency plan and call emergency services. Keep the packaging, contact the retailer or manufacturer for a refund, and read the official recall notice for the exact allergen.

Is the Merical, LLC recall still active?

The FDA lists this recall as recall closed. It remains relevant if you still have the affected product or need to identify a historical recall.

Where can I verify this recall?

This page is normalized from the openFDA enforcement record F-0631-2020. You can verify it directly using the official source link on this page. VerifyRecall updates its index from public FDA enforcement data and does not replace advice from the FDA, the recalling firm or a healthcare professional.

Verify before you act.

VerifyRecall is independent and not affiliated with the FDA. Always confirm the latest status on the official source record.

Official source

Brand history

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Record last synced from official openFDA enforcement data on November 14, 2026. Source record: official FDA notice.