Check the Batch
Class IITerminated in FDA datasetRecall initiated Jan 9, 2020

Meijer Joint Health Movement Advanced Dietary Supplement with Glucosamine + Chondroitin. 1500…

Recalling firm: Merical, LLC

Why it was recalled

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

Historical recall record. This is not a new recall announcement. “Terminated” describes the FDA recall process; it does not certify that an individual package is safe. FDA termination date: Aug 14, 2020.

Check your package

Compare the exact product and package details with the label you have.

ProductMeijer 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
UPC713733562966

FDA code information

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

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Full FDA record and distribution details

Original product description

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

Extracted codes and context

TypeCode / valueContext
UPC713733562966 Unit Size - 80 count - 2 tablets per day. Item Numbers: MEIJER7383 UPC Code: 713733562966 Distributed by Meijer Distribution Inc. Grand Rapids, MI

Original FDA recall reason

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

Recall details

Recall number
F-0632-2020
Event ID
84690
FDA status
Terminated
Initiated
Jan 9, 2020
Reported
Feb 12, 2020
Classified
Feb 4, 2020
Terminated
Aug 14, 2020
Quantity
977 cases
Location
Orange, CA, United States
Initiation type
Voluntary: Firm initiated
Notification
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit

Where it was distributed

one customer , corporate in MI.

FDA source record · F-0632-2020

Data updated September 16, 2026. View official FDA data ↗

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