FDA Recall United States TerminatedTerminated: August 14, 2020Historical recordClass II
Merical, LLC
- Product
- Meijer Joint Health Movement Advanced Dietary Supplement wi…
- Published
- February 12, 2020
- Distribution
- one customer , corporate in MI.
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 Triple Strength Formula Glucosamine Hydrochloride 1500 mg; Helps Overall Joint Physical Function; Unit Size - 40 count and 80 count - 2 tablets per day. Item Numbers: MEIJER7754 (40 count) & MEIJER7755 (80 count) UPC Code: 713733563024 & 713733563031 respectively Distributed by Meijer Distribution Inc. Grand Rapids, MI | Not published in this source record | 2596 Packaged Cases | 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 |
This recall shares FDA event ID 84690 with 1 other product entry in Public Health Trace.
FDA Recall United States TerminatedTerminated: August 14, 2020Historical recordClass II
Responsible company: Merical, LLC
FDA Recall United States OngoingHistorical recordClass I
FDA Recall United States TerminatedTerminated: August 14, 2020Historical recordClass II
FDA Recall United States TerminatedTerminated: March 6, 2020Historical 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:
FDA classifies this recall as Class II. See how to read an FDA recall record (linked above) for what each classification level means.
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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This record is preserved as published by FDA, as of August 14, 2020.
Status as reported: Terminated.
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