Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.
Reason for recall: Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products. Distribution: US Nationwide distribution including Puerto Rico. Quantity: 347422 units Lot/code info: UDI/DI 14026704341167, Batch Numbers: 18FT35, 18GG16, 18GG19, 18GG23, 18GG34, 18GT32, 18HG17, 18HG21, 18HG22, 18HG29, 18HG30, 18IG15, 18JG01, 18JG03, 18JG16, 18JG19, 18JG35, 18JG37, 18KG17, 18KG19, 18KG38, 18LG12, 18LG14, 18LG18, 18LG30, 19AG01, 19AG19, 19AG29, 19BG18, 19BG32, 19BG33, 19CG01, 19CG02, 19CT26, 19CT33, 19CT53, 19CT73, 19CT80, 19CT82, 19DT05, 19DT30, 19DT35, 19DT38, 19DT42, 19ET18, 19ET34, 19ET39, 19ET40, 19ET58, 19ET60, 19ET61, 19ET65, 19ET69, 19FT01, 19FT41, 19GT13, 19GT16, 19GT63, 19HT31, 19HT82, 19IT01, 19IT14, 19JT35, 19JT56, 19JT63, 19KT02, 19KT41, 19KT46, 19LT21, 19LT36, 20AT22, 20AT53, 20BT01, 20BT02, 20CT05, 20DT23, 20DT29, 20DT32, 20DT35, 20ET04, 20ET33, 20ET34, 20ET38, 20ET39, 20FT17, 20FT19, 20FT60, 20FT64, 20FT68, 20GT11, 20GT34, KME20H1786, KME20H2999, KME20J0367, KME20J0494, KME20J1209, KME20J1388, KME20M2796, KME20M2906, KME20M2907, KME20M2994, KME20M3092, KME21A1005, KME21A1006, KME21A2030, KME21A2037, KME21A3023, KME21A3024, KME21A3028, KME21A3029, KME21B0259, KME21B0788, KME21B0994, KME21B1198, KME21B1286, KME21B1288, KME21B1620, KME21B2627, KME21B2628, KME21B2705, KME21C0428, KME21C1121, KME21C1199, KME21C1879, KME21C3336, KME21F0980, KME21K1094, KME21K1655, KME21K1714, KME21K1841, KME21K2300, KME21K3006, KME21L2290, KME21L2744, KME21L2745, KME21L2760, KME21L2761, KME21L2787, KME21L2869, KME21M0203, KME21M0801, KME21M0809, KME21M0950, KME21M1706, KME21M1904, KME21M1905, KME21M2908, KME22A0561, KME22A2283, KME22A2404, KME22A2849, KME22A2915, KM
14026704341167
Official record: FDA (Device enforcement) ↗
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