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RECALL RECORD — CLASS IIRecall closedF-0632-2020/FDA enforcement
Merical, LLC·Dietary Supplements·Jan 9, 2020

Meijer Joint Health Movement Advanced Dietary Supplement with Glucosamine + Chondroitin

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

    Stop taking the supplement. Check the lot and UPC codes below, then return it to the retailer or contact the manufacturer about a refund. Seek medical advice if you have concerns about exposure.

Recall closed · classified by the FDAIN, MIMore supplements

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Product identification

Source: FDA FOOD

Brand nameMerical, LLC
Recalling firmMerical, LLCOrange, CA, United States
UPC / barcodes
7 13733 56296 6
Lot / date codes
  • 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
Distribution area
INMI

one customer, corporate in MI.

United States

Quantity affected977 cases
Recall initiationFDA report date: February 12, 2020
FDA recall numberF-0632-2020

Beyond the headline

The recall, in context

Merical, LLC initiated this supplements 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 Movement Advanced Dietary Supplement with Glucosamine + Chondroitin was made or distributed by Merical, LLC in Orange, CA, United States. This page reflects FDA report F-0632-2020, 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 Movement Advanced Dietary Supplement with Glucosamine + Chondroitin recall?

Merical, LLC recalled Meijer Joint Health Movement Advanced Dietary Supplement with Glucosamine + Chondroitin in an FDA Class II enforcement action reported as F-0632-2020. Product label does not contain Crustacean Shellfish on the ingredient list or allergen information

What should I do if I bought this product?

Stop taking the supplement. Check the lot and UPC codes below, then return it to the retailer or contact the manufacturer about a refund. Seek medical advice if you have concerns about exposure. 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-0632-2020. 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

More recalls by Merical, LLC

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

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