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FDA (Device enforcement)Recalled 2023-11-06class i

Nurse Assist, LLC: Sterile Water/Saline: Brand Name: Product Name/Product Code: CARDINAL: 100ML STERILE SALINE BOTTLE/1020, 100ML STERILE SALINE BOTTLE/1022, 100ML STERILE WATER BOTTLE/1024, 100ML STE

Hazard

Sodium chloride irrigation USP, and sterile water for irrigation USP, that may be packaged inside kits, have the potential for a lack of sterility assurance, which could result in a nonsterile product, use of which could cause infection.

Details from the source

Reason for recall: Sodium chloride irrigation USP, and sterile water for irrigation USP, that may be packaged inside kits, have the potential for a lack of sterility assurance, which could result in a nonsterile product, use of which could cause infection. Distribution: US Nationwide Distribution: SC AZ, CA, FL, GA, HI, IA, IN, KS, KY, MA, ME, MN, MS, NC, ND, NE, NJ, NV, NY, OH, PA, RI, TX, WA, WI, AK, AL, AR, CO, CT, DC, ID, IL, LA, MD, MI, MO, MT, NH, NM, OK, OR, PR, SD, TN, UT, VA , WI, WV, WY. OUS (foreign) distribution to: Canada Quantity: 31,850 Cases Lot/code info: Product Code/UDI-DI/Lot: 1020/50192253044490/21122619, 22063546, 22094023, 22094028, 22094074, 22094095, 22104138, 23045320, 23076080; 1022/50192253044506/22012651, 22063553, 22083775, 22093943, 22094062, 22104137, 23045338, 23076038, 23076088; 1024/50192253044513/21122618, 22073561, 22093989, 22094122, 23034994, 23045174, 23076031, 23076098; 10000/50192253044520/22073713, 22094086, 22104147, 22104279, 23076079; PT00103419/50192253044513/23076122; PT00103427/50192253044506/23076140, 23086258; 90SAL/20884521140940/22083848; 210SAL/10884521139756/22022771, 22022776, 22114334; 49148/20885632395878/23076067; 49152/20885632395915/23076041; 49154/20885632395939/23076066; 49155/20885632395946/23076057; 49150/20885632395892/23076074; 49151/20885632395908/23076040; 49149/20885632395885/23086163 49153/20885632395922/23086156; 98-09444-01/21112440, 22032932, 22083886, 22104140, 22114339, 22114360, 23065971, 23096487; 37-6240/612479168565/21112357, 21122528, 21122548, 21122575, 21122592, 22012685, 22012686, 22022799, 22022851, 22032904, 22033051, 22043170, 22053283, 22053288, 22053289, 22053320, 22053340, 22053350, 22063460, 22063544, 22073632, 22073677, 22073611, 22083819, 22083851, 22083875, 22083918, 22093952, 22093941, 22093979, 22094096, 22104150, 22104165, 22114282, 22114389, 23014636, 23014707, 23014774, 23024917, 23034942, 23035016, 23035030, 23035064, 23035081, 23035118, 23035140, 23045190, 23045208, 23045264, 23045283, 23055541, 23065812, 23065878, 23065912, 23065939, 23075988,

UPC codes

50192253044490, 50192253044506, 50192253044513, 50192253044520, 20884521140940, 10884521139756, 20885632395878, 20885632395915, 20885632395939, 20885632395946, 20885632395892, 20885632395908, 20885632395885, 20885632395922, 612479168565, 612479180314, 612479168596, 612479180307, 612479168541, 612479228399, 612479228405, 612479168558, 612479168572, 612479168589, 612479133761, 612479228429, 50885632127043, 40884389334233, 40884389338248, 40080196427056, 40884389338262, 40884389118390, 40884389118406, 40884389338231, 40080196297970, 40884389334226, 10850421008751, 10850421008812, 10850421008768, 10850421008829

Source

Official record: FDA (Device enforcement)

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

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