TELEFLEX LLC recalls Endotracheal Tube oral/nasal Murphy Eye, High Volume, Low Pr
Recalled Product
Endotracheal Tube oral/nasal Murphy Eye, High Volume, Low Pressure Cuff, REF 112082085
Hazard / Issue
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.
Issued by
FDA
Distribution: Nationwide (United States)
Lot/Code Info: UDI/DI 14026704341457, Batch Numbers: 18HG37, 18HT15, 18HT24, 18JG12, 18JG31, 19CT69, 19CT73, 19CT74, 19CT76, 19CT77, 19DT05, 19DT10, 19KT14, 19KT30, 19KT46, 19KT49, 19KT50, 19KT55, 19LT35, 20BT51, 20CT02, 20CT22, 20CT28, 20CT32, 20CT42, 20DT02, 20DT17, 20DT18, 20ET17, 20GG43, KME20H0750, KME20J2539, KME20J2680, KME20K0923, KME20K1114, KME20K1513, KME20K3034, KME20K3146, KME20L1867, KME20L2274, KME20M1511, KME21E0902, KME21F0741, KME21F1214, KME21F2006, KME21F2074, KME21K0095, KME21K1193, KME21K2275, KME21K2575, KME21K3015, KME21L0394, KME21L0799, KME21L1115, KME21L1276, KME21L1586, KME21M2500, KME21M2728, KME22A0787, KME22A2287, KME22A2957, KME22A2968, KME22B0519, KME22B1154, KME22B1696, KME22B1775, KME22B2179, KME22B2320, KME22B2477, KME22B2797, KME22C2074, KME22D1891, KME22D1892, KME22D3186, KME22D3488, KME22D3564, KME22E0663, KME22E0988, KME22E1279, KME22E1583, KME22E1811, KME22E2253
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