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…
Recalling firm: Merical, LLC
Why it was recalled
Product label does not contain Crustacean Shellfish on the ingredient list or allergen information
The exact product
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
Check the codes
Compare these FDA-provided codes, lot numbers or dates with the product you have.
Match the product, size and code together. A similar name alone does not identify your batch.
Original 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
| Type | Code / value | Context |
|---|---|---|
| UPC | 713733562966 | Unit Size - 80 count - 2 tablets per day. Item Numbers: MEIJER7383 UPC Code: 713733562966 Distributed by Meijer Distribution Inc. Grand Rapids, MI |
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.
Data updated September 16, 2026. View official FDA data ↗
A missing code match is not a guarantee of safety. Follow official FDA and manufacturer guidance.