FDA Recall United States Terminated Historical recordClass II
Merical, LLC
- Product
- Meijer Joint Health Movement Advanced Dietary Supplement wi…
- Published
- February 12, 2020
- Distribution
- one customer , corporate in MI.
Merical, LLC Recall: Product label does not contain Crustacean Shellfish on the ingredient list or allergen information
United States
TerminatedClass II
- Company
- Merical, LLC
- Product
- Meijer Joint Health Triple Strength Formula Glucosamine Hyd…
- Recall date
- January 9, 2020
- Terminated
- August 14, 2020
- Source
- FDA
Reason for recall
Product label does not contain Crustacean Shellfish on the ingredient list or allergen information
- - Recall initiated
- - Reported by source
- - Recall terminated
| 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 |
Distribution
- one customer
- corporate in MI.
Official source record
- Agency
- FDA
- Dataset
- FDA Food Enforcement (Recalls)
- Recall number
- F-0631-2020
- Event ID
- 84690
- Status
- Terminated
- Classification
- Class II
- Company
- Merical, LLC
- Product description
- 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
- Quantity
- 2596 Packaged Cases
- Reason
- Product label does not contain Crustacean Shellfish on the ingredient list or allergen information
- Recall initiation date
- January 9, 2020
- Report date
- February 12, 2020
- Classification date
- Not published in this source record
- Termination date
- August 14, 2020
- Distribution pattern
- one customer , corporate in MI.
- UPC, lot, and code information
- 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
- Voluntary or mandated
- Voluntary: Firm initiated
- Initial notification method
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
- Source last updated
- Not tracked separately from the Public Health Trace retrieval date below
- Public Health Trace retrieval date
Other products recalled under this same event
This recall shares FDA event ID 84690 with 1 other product entry in Public Health Trace.
Responsible company: Merical, LLC
Other recalls from Merical, LLC
FDA Recall United States Ongoing Historical recordClass I
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- Product
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- Published
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- Distribution
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FDA Recall United States Terminated Historical recordClass II
Merical, LLC
- Product
- Meijer Joint Health Movement Advanced Dietary Supplement wi…
- Published
- February 12, 2020
- Distribution
- one customer , corporate in MI.
FDA Recall United States Terminated Historical recordClass III
Merical, LLC
- Product
- Leader Advanced Probiotic with 6 Probiotic Strains and 20 bi…
- Published
- December 4, 2019
- Distribution
- Nationwide
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.
Where this information comes from
View FDA enforcement record -- the specific openFDA record this summary was built from.
No separate FDA public notice was found for this enforcement record. The information below comes from FDA's Recall Enterprise System through openFDA.
FDA Enforcement Reports -- FDA's general, official recall and enforcement information.
Technical source data
View raw source data -- the machine-readable record this page's information was built from.
Retrieved by Public Health Trace:
Frequently asked questions
What does a Class II mean?
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.
Is this recall still active?
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.
What should I do if I have this product?
Follow the instructions published by the responsible agency (see the source links below) -- recall guidance (e.g. dispose of the product, return it for a refund, or check for a specific lot number) varies by recall and is set by that agency, not by Public Health Trace.
Where can I find more official information?
The source links below, published by FDA, are the authoritative record for this recall, including any updates issued after this summary was retrieved.
This summary is based on the official source record referenced above. Public Health Trace does not state that any company or product is unsafe beyond what the official source has published. Read the full medical disclaimer.
