TELEFLEX LLC recalls Preformed AGT Oral Endotracheal Tube Murphy Eye, High Volume
Recalled Product
Preformed AGT Oral Endotracheal Tube Murphy Eye, High Volume, Low Pressure Cuff, REF 111780045
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 14026704341051, Batch Numbers: 18FG12, 18GG26, 18GT26, 18HG24, 18HG36, 18JG13, 18JG36, 18LG31, 18LG33, 19AG11, 19AG21, 19CG07, 19DT42, 19FT18, 19GT43, 19JT02, 19KT37, 19LT32, 20AT13, 20BT53, 20CT21, 20DT15, 20ET50, 20FT36, 20FT60, 20GG43, 20GT40, KME20K2722, KME20K2733, KME20L0659, KME20L1620, KME20M0897, KME20M1522, KME21A0198, KME21A0967, KME21A2397, KME21B2435, KME21C0325, KME22C1814, KME22C1815, KME22C2815, KME22D1075, KME22D3468, KME22E0686, KME22E2786, KME22F1459, KME22G0186, KME22G0338, KME22H1790, KME22J0267, KME22J1449, KME22J2193, KME22J2455, KME22K0574, KME22M1047, KME22M1305, KME22M1323, KME22M2819, KME22M3040, KME23A2332, KME23A2894, KME23A2895, KME23A3034
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