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 112082060
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 14026704341402, Batch Numbers: 18GG13, 18GG15, 18HG07, 18HG30, 18IG06, 18IG14, 18IG27, 18IT06, 18IT18, 18IT25, 18JT06, 19CG03, 19CT25, 19CT29, 19CT45, 19CT50, 19CT61, 19CT76, 19DT05, 19DT14, 19GT07, 19HT61, 19IT05, 19IT12, 19IT33, 19IT43, 19IT55, 19IT59, 19JT30, 19KT07, 19KT31, 19LT04, 19LT08, 20AT41, 20AT49, 20BT39, 20BT46, 20BT51, 20CT13, 20CT54, 20ET12, 20ET15, 20ET16, 20ET17, 20FT23, 20FT45, 20GT09, 20GT34, 20GT38, KME20J0548, KME20J1458, KME20J2801, KME20K0435, KME20K1112, KME20K2168, KME20L1143, KME20L1420, KME20L2089, KME20L2783, KME20M0663, KME20M1064, KME20M1143, KME21E0660, KME21G0572, KME21G1976, KME21G2260, KME21H0911, KME21H1123, KME21K0411, KME21K0550, KME21L0214, KME21L0952, KME21L2133, KME21L2271, KME21M2791, KME21M2792, KME22A1454, KME22A1518, KME22A2004, KME22A2431, KME22A2484, KME22A2892, KME22A2958, KME22B0288, KME22B0499, KME22B1509, KME22B1895, KME22C0832, KME22D2180, KME22D3181, KME22E0328, KME22E0977, KME22F0005, KME22F0189, KME22F0762, KME22F1398, KME22F2154, KME22F3471, KME22G0140, KME22G0188, KME22G2351, KME22G2656, KME22G3065, KME22G3236, KME22H0773, KME22H0828, KME22H1589, KME22J1998, KME22K0733, KME22K0898, KME22K0991, KME23B0877
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