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: 302652 units Lot/code info: UDI/DI 14026704341181, Batch Numbers: 18FG31, 18FT35, 18FT39, 18GG17, 18GG18, 18GT32, 18HG17, 18HG19, 18HG21, 18HG22, 18HG29, 18IG15, 18IG17, 18IG30, 18JG16, 18JG19, 18JG35, 18JG37, 18KG17, 18KG39, 18KG40, 18LG14, 18LG15, 18LG18, 18LG39, 19AG25, 19BG02, 19BG04, 19BG18, 19BG19, 19BG32, 19CG01, 19CT28, 19CT33, 19CT36, 19CT56, 19CT57, 19CT80, 19DT05, 19DT30, 19ET34, 19ET36, 19ET39, 19ET40, 19ET61, 19ET65, 19FT01, 19FT45, 19GT13, 19GT63, 19HT24, 19HT31, 19HT53, 19IT54, 19JT06, 19JT10, 19JT11, 19JT14, 19JT35, 19JT63, 19KT14, 19KT38, 19KT41, 19KT46, 19LT17, 19LT21, 20AT22, 20BT53, 20CT07, 20CT12, 20CT14, 20CT32, 20DT18, 20DT29, 20ET34, 20ET38, 20ET49, 20FT17, 20FT19, 20FT21, 20FT64, 20GT11, KME20J0370, KME20J0663, KME20J0665, KME20J1212, KME20K3628, KME20L2213, KME20L2286, KME20L2666, KME20L2668, KME20M0644, KME20M1284, KME20M2643, KME20M2645, KME20M2956, KME20M3015, KME21A1024, KME21A1065, KME21A1273, KME21A2079, KME21A2235, KME21A3066, KME21B0255, KME21B0256, KME21B0378, KME21B2209, KME21B2274, KME21B2275, KME21B2535, KME21C0433, KME21C0643, KME21C1123, KME21C1125, KME21C1164, KME21E0006, KME21F0902, KME21F1216, KME21F2139, KME21F2198, KME21J0892, KME21J1496, KME21J1690, KME21J1813, KME21J2074, KME21K0004, KME21K0115, KME21K0296, KME21K0875, KME21K0877, KME21K1029, KME21K1079, KME21K1716, KME21K1826, KME21K1868, KME21K2303, KME21K2335, KME21K3007, KME21L0889, KME21L0985, KME21L1526, KME21L1597, KME21L1776, KME21L2153, KME21L2154, KME21L2299, KME21L2885, KME21M0162, KME21M0337, KM
14026704341181
Official record: FDA (Device enforcement) ↗
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