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 111780070
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 14026704341105, Batch Numbers: 18FG12, 18FG24, 18GG01, 18GG26, 18GT26, 18HG36, 18IG14, 18IT05, 18JG07, 18KG10, 18KG34, 18LG11, 18LG31, 19AG36, 19CG07, 19CT69, 19ET12, 19GT39, 19GT44, 19HT80, 19IT12, 19IT43, 19JT01, 19JT55, 19KT21, 19LT08, 19LT31, 20AT13, 20AT49, 20BT53, 20CT24, 20DT09, 20DT24, 20ET50, 20FT39, 20FT59, 20GG27, KME20J2813, KME20J3155, KME20K1111, KME20K2068, KME20K3244, KME20L0730, KME20L0731, KME20L1681, KME20M0276, KME20M0955, KME20M2655, KME21A0979, KME21B0096, KME21B0154, KME21B1518, KME21C0334, KME21M1046, KME22A0450, KME22A1594, KME22B0425, KME22B1002, KME22C0473, KME22D1110, KME22D2351, KME22D2363, KME22D3366, KME22D3379, KME22E1102, KME22E2443, KME22F1333, KME22G0171, KME22G1728, KME22G3156, KME22H0815, KME22H1321, KME22J0749, KME22K1286, KME22K2440, KME22L1550, KME22L1660, KME22L2544
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