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: 446163 units Lot/code info: UDI/DI 14026704341174, Batch Numbers: 18FG33, 18GG16, 18HG17, 18HG21, 18HG29, 18HG30, 18HG31, 18IG10, 18IG14, 18IG17, 18IG20, 18JG02, 18JG03, 18JG16, 18JG19, 18JG20, 18JG35, 18JG37, 18KG01, 18KG17, 18KG19, 18KG36, 18KG39, 18KG41, 18LG12, 18LG14, 18LG30, 18LG39, 19AG01, 19AG17, 19AG19, 19AG29, 19BG02, 19BG18, 19BG19, 19BG32, 19BG33, 19CG01, 19CT26, 19CT33, 19CT53, 19CT56, 19CT80, 19DT05, 19DT30, 19DT46, 19ET18, 19ET34, 19ET39, 19ET40, 19ET61, 19ET65, 19ET69, 19FT01, 19FT41, 19GT13, 19HT68, 19IT01, 19IT15, 19IT53, 19IT54, 19JT06, 19JT10, 19JT14, 19JT56, 19JT63, 19KT02, 19KT14, 19KT38, 19KT41, 19LT16, 19LT21, 19LT36, 20AT22, 20BT02, 20CT02, 20CT05, 20CT11, 20CT14, 20CT32, 20DT19, 20DT20, 20DT23, 20DT29, 20DT32, 20DT35, 20ET33, 20ET34, 20ET38, 20ET39, 20ET49, 20FT17, 20FT18, 20FT60, 20GT34, KME20H0612, KME20H1787, KME20H2570, KME20H2572, KME20H2573, KME20H3001, KME20H3127, KME20H3128, KME20J1211, KME20J1389, KME21A1007, KME21A1008, KME21A1182, KME21A2025, KME21A2026, KME21A2189, KME21A3059, KME21A3060, KME21A3083, KME21A3084, KME21B0258, KME21B0790, KME21B1083, KME21B1259, KME21B1289, KME21B1545, KME21B1605, KME21B1754, KME21B2217, KME21B2530, KME21B2672, KME21C0424, KME21C0425, KME21C2416, KME21J1495, KME21K1633, KME21K1715, KME21K1842, KME21K1866, KME21K2302, KME21K2458, KME21K2459, KME21K2495, KME21K2579, KME21K2998, KME21K3000, KME21K3001, KME21L0074, KME21L0890, KME21L1033, KME21L1359, KME21L1364, KME21L1365, KME21L1435, KME21L1525, KME21L2143, KME21L2788, KME21M0949, KME21M
14026704341174
Official record: FDA (Device enforcement) ↗
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