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FDA (Device enforcement)Recalled 2024-03-22class ii

MEDLINE INDUSTRIES, LP - Northfield: Medline medical procedure kits labeled as follows: a) ARTHROSCOPY, REF DYNJ909699; b) BACK CDS, REF CDS984000C; c) EXTREMITY, REF DYNJ900847A; d) HAND-LF, REF DYNJ

Hazard

A slight dimensional variation which has the potential for increased difficulty fitting into outer canister.

Details from the source

Reason for recall: A slight dimensional variation which has the potential for increased difficulty fitting into outer canister. Distribution: Worldwide - US Nationwide and the countries of Panama, Mexico, Canada, Qatar, El Salvador, Oman, Colombia, Singapore. Quantity: 14977 units Lot/code info: a) REF DYNJ909699, UDI/DI 40195327446759 (case), 10195327446758 (unit), Lot Numbers: DYNJ909699, DYNJ909699, DYNJ909699, DYNJ909699, DYNJ909699, DYNJ909699; b) REF CDS984000C, UDI/DI 40889942011552 (case), 10889942011551 (unit), Lot Numbers: 22GBT604, 22IBI040, 23ABA955, 23DBT170, 23EBU747, 23HBB409; c) REF DYNJ900847A, UDI/DI 40888277771209 (case), 10888277771208 (unit), Lot Numbers: d) REF DYNJ902619G, UDI/DI 40195327214488 (case), 10195327214487 (unit), Lot Numbers: 22FBG650, 22FBK152, 22FBW287, 22HBA416, 22HBG372, 22HBS529, 22JBA184, 23EBC466, 23HBL953; e) REF CDS984009C, UDI/DI 40888277768971 (case), 10888277768970 (unit), Lot Numbers: 22FBL426, 22GBU282, 23CBD236, 23HBY917; f) REF DYNJ902380K, UDI/DI 40195327507009 (case), 10195327507008 (unit), Lot Numbers: 23KBX257; g) REF DYNJ904771B, UDI/DI 40195327137190 (case), 10195327137199 (unit), Lot Numbers: 22EMB001, 22IMF542, 22KMC063, 23AME421, 23CMC716, 23DME033, 23FMI125, 23HMC273, 23HMI602, 23LME735; h) REF DYNJ905519D, UDI/DI 40193489967396 (case), 10193489967395 (unit), Lot Numbers: 22GMG221, 22HMB217, 22LMJ233, 23AME962, 23AMI318, 23AMJ640, 23DMI673, 23IMG465, 23LMD163; i) REF DYNJ906273F, UDI/DI 40195327511013 (case), 10195327511012 (unit), Lot Numbers: 23JBH985; j) REF DYNJ909747, UDI/DI 40195327468201 (case), 10195327468200 (unit), Lot Numbers: 23HBZ535, 23KBF559; k) REF DYNJS2029D, UDI/DI 40193489214414 (case), 10193489214413 (unit), Lot Numbers: 22IDA884, 22LDA526, 23CDA885, 23FDA459, 23JDB741; l) REF DYNJ907159

UPC codes

40195327446759, 10195327446758, 40889942011552, 10889942011551, 40888277771209, 10888277771208, 40195327214488, 10195327214487, 40888277768971, 10888277768970, 40195327507009, 10195327507008, 40195327137190, 10195327137199, 40193489967396, 10193489967395, 40195327511013, 10195327511012, 40195327468201, 10195327468200, 40193489214414, 10193489214413, 40193489970419, 10193489970418, 40889942850953, 10889942850952, 40195327040407, 10195327040406, 40195327511228, 10195327511227, 40195327511235, 10195327511234, 40195327510986, 10195327510985, 40195327137039, 10195327137038, 40193489967549, 10193489967548, 40195327468225, 10195327468224

Source

Official record: FDA (Device enforcement)

Republished from the official source above; details can change — the source record controls.

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