TELEFLEX LLC recalls Preformed AGT Oral Endotracheal Tube Murphy Eye, High Volume

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/I 14026704341150, Batch Numbers: 18FG20, 18FG31, 18GG23, 18GG34, 18GT32, 18HG17, 18IG15, 18JG01, 18JG16, 18JG35, 18KG17, 18KG18, 18KG36, 18LG15, 18LG30, 18LG39, 19AG15, 19BG33, 19CG01, 19CG02, 19CT26, 19DT03, 19DT30, 19DT38, 19ET58, 19ET69, 19FT37, 19FT46, 19IT53, 19JT10, 19KT14, 19KT46, 19LT16, 20AT22, 20AT26, 20CT11, 20CT32, 20DT19, 20DT32, 20ET34, 20ET49, 20FT18, 20FT64, 20GT11, KME20H0466, KME20H2769, KME20H2998, KME20H3129, KME20M0650, KME20M1283, KME20M2799, KME20M2822, KME21A2028, KME21A3020, KME21B1044, KME21B1197, KME21B1960, KME21B1961, KME21C0324, KME21C0426, KME21C1119, KME21L0024, KME21L0026, KME21L1782, KME21L2301, KME21L2785, KME21M1710, KME21M2600, KME21M2601, KME22A0560, KME22A0755, KME22A1376, KME22C0493, KME22D1697, KME22D2626, KME22D2999, KME22D3173, KME22D3253, KME22E0727, KME22E0728, KME22E1011, KME22E1155, KME22E1392, KME22E2151, KME22E2239, KME22E2744, KME22E2753, KME22F0075, KME22F0229, KME22F0540, KME22F0600, KME22F0880, KME22F1315, KME22F1736, KME22F2068, KME22F2353, KME22F2627, KME22F2949, KME22F3119, KME22F3242, KME22F3425, KME22G0214, KME22G0600, KME22G0898, KME22G1642, KME22G1861, KME22G2270, KME22G3150, KME22G3268, KME22H2027, KME22H3065, KME22H3272, KME22H3273, KME22H3400, KME22J0633, KME22J0901