FDA recall record
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....
FDA classification. FDA Class I, II, and III are not the same as USDA FSIS classifications and are not a cross-agency safety score.
FDA listed a termination date of August 14, 2020. openFDA does not treat this as a live recall-status tracker.
Product described in an FDA recall
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
Reason
Product label does not contain Crustacean Shellfish on the ingredient list or allergen information
Products involved
Product descriptions are copied from the FDA recall record. They are not a current catalog and are not automatically matched to WhoMadeMyFood product pages.
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
Code information listed by FDA
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 and firm information
Recalling firm listed by FDA: Merical, LLC
Firm location listed by FDA: Orange, CA, United States
Distribution reported by FDA: one customer , corporate in MI.
Product quantity listed by FDA: 2596 Packaged Cases
Source
Source: U.S. Food and Drug Administration (FDA), openFDA food enforcement reports.
Official FDA openFDA food enforcement record
Identifying an FDA recall record does not imply FDA endorsement of WhoMadeMyFood. Methodology.