FDA Recall United States Terminated Historical recordClass II
Merical, LLC
- Product
- Meijer Joint Health Triple Strength Formula Glucosamine Hyd…
- Published
- February 12, 2020
- Distribution
- one customer , corporate in MI.
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United States
TerminatedClass II
Product label does not contain Crustacean Shellfish on the ingredient list or allergen information
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| 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 | Not published in this source record | 977 cases | 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 |
This recall shares FDA event ID 84690 with 1 other product entry in Public Health Trace.
FDA Recall United States Terminated Historical recordClass II
Responsible company: Merical, LLC
FDA Recall United States Ongoing Historical recordClass I
FDA Recall United States Terminated Historical recordClass II
FDA Recall United States Terminated Historical recordClass III
A map highlighting the states named in the source's distribution description.
Shading reflects state-level totals only, as published by the source. It does not imply county-level or point-level precision.
| State | Distributed |
|---|---|
| Michigan | 1 |
States shown are extracted from the source's free-text distribution description above; a narrative description (e.g. "distributed nationwide") may not list individual states to extract.
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Retrieved by Public Health Trace:
A situation in which use of or exposure to a product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote.
According to FDA, this recall's status is "Terminated." Always confirm the current status using the source links below, since status can change after Public Health Trace last retrieved this record.
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