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 112082055
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 14026704341396, Batch Numbers: 18FG33, 18FT26, 18GG13, 18GG15, 18GG25, 18GT11, 18GT34, 18HG28, 18IG05, 18IG14, 18JT04, 18KG25, 18KG26, 18LG19, 18LG40, 19AG19, 19AG32, 19AG33, 19ET31, 19ET73, 19JT36, 19KT18, 20AT32, 20AT40, 20BT10, 20BT38, 20CT54, 20ET17, 20ET18, KME20G0395, KME20H0640, KME20J2829, KME20L1703, KME21A1433, KME21E0864, KME21E1230, KME21F0946, KME21F1967, KME21G0850, KME21J0319, KME21K1627, KME21M0312, KME22A2333, KME22A2942, KME22B0352, KME22B0563, KME22B1357, KME22C0323, KME22C2218, KME22C2923, KME22D0055, KME22D0282, KME22D0603, KME22D1799, KME22D3018, KME22E0652, KME22E1164, KME22F0418, KME22F0898, KME22F1662, KME22G0318, KME22G2350, KME22H0635, KME22H1516, KME22H1612, KME22J1044, KME22J1464, KME22J2331, KME22J2332, KME22K0635, KME22K0780, KME22K1440, KME23A2300, KME23A2432, KME23A2845, KME23A3010
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