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: 247645 units Lot/code info: UDI/DI 14026704341419, Batch Numbers: 18FG23, 18FG27, 18FG30, 18FG31, 18FT06, 18FT08, 18GG19, 18GT32, 18GT34, 18HG02, 18HG15, 18IG02, 18IG07, 18IG13, 18IT25, 18JG01, 18JG02, 18JG04, 18JG07, 18JG20, 18KG44, 18KT28, 18LG14, 19AG09, 19AG15, 19AG32, 19AG33, 19AT20, 19BG14, 19BG18, 19BG40, 19CG07, 19CT26, 19CT39, 19CT40, 19CT76, 19DT10, 19DT16, 19DT27, 19DT47, 19ET02, 19ET05, 19ET65, 19GT19, 19GT29, 19GT30, 19GT31, 19GT38, 19HT26, 19HT61, 19HT66, 19HT68, 19IT20, 19IT33, 19IT59, 19JT18, 19JT19, 19JT26, 19JT32, 19JT36, 19JT49, 19JT63, 19KT20, 19KT21, 19KT26, 19LT07, 19LT31, 19LT46, 20AT05, 20AT06, 20AT20, 20AT47, 20AT49, 20BT13, 20CT02, 20CT13, 20CT23, 20CT37, 20CT47, 20CT54, 20DT01, 20DT02, 20ET16, 20ET18, 20GT05, 20GT06, 20GT13, 20GT22, 20GT24, KME20H0882, KME20H2726, KME20H2934, KME20J1386, KME20J1399, KME20J1656, KME20K0036, KME20K0259, KME20K0436, KME20K0504, KME20K0677, KME20K0881, KME20L2349, KME20L2447, KME20L2448, KME20M0710, KME20M0892, KME20M0928, KME20M1806, KME20M1923, KME20M2249, KME20M2450, KME20M2708, KME21A0338, KME21A0404, KME21A0695, KME21B1352, KME21B2607, KME21B2789, KME21C0504, KME21C0981, KME21C0983, KME21C1035, KME21C1097, KME21E0607, KME21E0685, KME21F0384, KME21F0516, KME21F0694, KME21F0834, KME21F0930, KME21F1554, KME21F1885, KME21F2156, KME21F2203, KME21G0532, KME21H0202, KME21H0916, KME21H1233, KME21H1264, KME21J0302, KME21J0389, KME21J0528, KME21J0637, KME21J0725, KME21J0909, KME21J1871, KME21J1945, KME21J1998, KME21K0570, KME21K0587, KME21K0829, KME21L
14026704341419
Official record: FDA (Device enforcement) ↗
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