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FDA (Device enforcement)Recalled 2023-11-15class i

MEDLINE INDUSTRIES, LP - Northfield: Medline Kits, trays, and packs labeled as follows: a) 709E RECOVERY PACK A,B,C II SS, REF DYNJ55960G; b) ABDOMEN PACK, REF DYNJ53643C; c) BAG TRUNK STOCK KIT, REF

Hazard

Medline Industries, LP is recalling certain kits and trays that were manufactured using specific lots of Nurse Assist (as components): 0.9% Sodium Chloride Irrigation USP, Sterile Water for Irrigation USP and Saline Flush Syringe. Nurse Assist issued a recall due to the potential lack of sterility, which could result in the solution being non sterile.

Details from the source

Reason for recall: Medline Industries, LP is recalling certain kits and trays that were manufactured using specific lots of Nurse Assist (as components): 0.9% Sodium Chloride Irrigation USP, Sterile Water for Irrigation USP and Saline Flush Syringe. Nurse Assist issued a recall due to the potential lack of sterility, which could result in the solution being non sterile. Distribution: Distribution US nationwide including Puerto Rico, Canada, UAE, and Panama Quantity: 26171 units Lot/code info: a) REF DYNJ55960G, UDI/DI 40193489917827 (case), 10193489917826 (unit), Lot Numbers: 23ALA126; b) REF DYNJ53643C, UDI/DI 40889942615354 (case), 10889942615353 (unit), Lot Numbers: 22CLA226, 22ELA033, 22GLA633, 22JLA774, 23BLA613, 23ELA554, 23FLA005; c) REF DYKM1880, UDI/DI 40193489807524 (case), 10193489807523 (unit), Lot Numbers: 22FLA285, 23FLA657, 23HLA920; d) REF DYKE1601, UDI/DI 40889942956082 (case), 10889942956081 (unit), Lot Numbers: 23ABG889, 23BBN595, 23BBU202, 23FBA860, 23HBI592; e) REF DYNDH1242, UDI/DI 40889942598138 (case), 10889942598137 (unit), Lot Numbers: 22GLA574, 22KLA372, 22LLA696, 23ALA194, 23BLA985, 23CLA356, 23ELA844, 23FLA654, 23GLB027, 23HLA029, 23ILA700, 23JLB281; f) REF DYKE1840, UDI/DI 40195327105649 (case), 10195327105648 (unit), Lot Numbers: 22BBT072, 22EBU502, 22KBM213, 22LBH747; g) REF DYNJ37775F, UDI/DI 40888277906182 (case), 10888277906181 (unit), Lot Numbers: 22FDB681, 23ADC041, 23HDA605; h) REF DYNDL1350A, UDI/DI 40889942880486 (case), 10889942880485 (unit), Lot Numbers: 22GBH314, 23ABI645, 23BBL282, 23BBU137, 23EBM149, 23FBC531, 23GBJ019, 23HBD916; i) REF DYNDL1350AH, UDI/DI 40889942880486 (case), 10889942880485 (unit), Lot Numbers: 22GBH314, 23ABI645, 23BBL282, 23BBU137, 23EBM149, 23FBC531, 23GBJ019, 23HBD916; j) REF DYNDA2277A, UDI/DI 40195327004423 (case), 10195327003944 (unit), Lot Numbers: 21LBS528, 22ABD844, 22BBE910; k) REF DYNDA2277B, UDI/DI UDI/DI 40195327120796 (case), 10195327120795 (unit), Lot Numbers: 22CBP893, 22DBQ630, 22IB

UPC codes

40193489917827, 10193489917826, 40889942615354, 10889942615353, 40193489807524, 10193489807523, 40889942956082, 10889942956081, 40889942598138, 10889942598137, 40195327105649, 10195327105648, 40888277906182, 10888277906181, 40889942880486, 10889942880485, 40195327004423, 10195327003944, 40195327120796, 10195327120795, 40193489421256, 10193489421255, 40889942790617, 10889942790616, 40653160991503, 10653160991502, 40653160991558, 10653160991557, 40653160991541, 10653160991540, 40193489342575, 10193489342574, 40193489880190, 10193489880199, 40195327306503, 10195327306502, 40889942148098, 10889942148097, 40195327044207, 10195327044206

Source

Official record: FDA (Device enforcement)

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

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