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: 172721 units Lot/code info: UDI/DI 14026704341198, Batch Numbers: 18FT35, 18FT39, 18GG17, 18GG18, 18GT32, 18IG10, 18IG16, 18IG17, 18JG13, 18JG20, 18JG35, 18JG37, 18KG18, 18KG39, 18KG41, 18LG12, 18LG14, 18LG30, 18LG39, 19AG29, 19BG03, 19BG04, 19BG18, 19BG19, 19BG33, 19CG01, 19CG02, 19CG04, 19CT28, 19CT33, 19CT56, 19DT03, 19DT30, 19DT35, 19DT42, 19DT46, 19ET16, 19ET34, 19FT01, 19GT63, 19HT31, 19HT55, 19IT01, 19IT12, 19IT14, 19IT15, 19IT19, 19KT02, 19KT41, 19LT17, 20BT01, 20BT02, 20CT07, 20DT18, 20DT29, 20DT32, 20ET34, 20ET49, 20FT18, 20FT64, 20GT11, 20GT34, 20GT49, KME20H0487, KME20H1788, KME20H2574, KME20H2768, KME20H3002, KME20J1213, KME20L0905, KME20L2170, KME20L2191, KME20L2670, KME20M0304, KME20M2647, KME20M3094, KME21A1082, KME21A2080, KME21A2926, KME21B0543, KME21B1199, KME21B1630, KME21B1716, KME21B2541, KME21B2670, KME21C0592, KME21C0593, KME21C3340, KME21D2002, KME21E0008, KME21E0009, KME21F0901, KME21F1424, KME21F1459, KME21F2371, KME21J1239, KME21J1487, KME21J1691, KME21J1692, KME21J1854, KME21K0178, KME21K1046, KME21K1078, KME21K2304, KME21K3005, KME21L0631, KME21L0756, KME21L1428, KME21L1429, KME21L1596, KME21L2141, KME21L2291, KME21L2736, KME22A1889, KME22A1890, KME22A2018, KME22A2281, KME22A2921, KME22A2969, KME22B0359, KME22C0207, KME22C2843, KME22C2927, KME22C2969, KME22C3213, KME22C3304, KME22C3375, KME22C3379, KME22D0052, KME22D0587, KME22D0719, KME22D0808, KME22D0844, KME22D0846, KME22D0855, KME22D0899, KME22D1001, KME22D1093, KME22D1115, KME22D1337, KME22D1348, KME22D1454, KME22D1568
14026704341198
Official record: FDA (Device enforcement) ↗
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