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FDA (Device enforcement)Recalled 2023-05-25class i

TELEFLEX LLC: Endotracheal Tube oral/nasal Murphy Eye, High Volume, Low Pressure Cuff, REF 112082085

Hazard

Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.

Details from the source

Reason for recall: Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products. Distribution: US Nationwide distribution including Puerto Rico. Quantity: 39550 units Lot/code info: UDI/DI 14026704341457, Batch Numbers: 18HG37, 18HT15, 18HT24, 18JG12, 18JG31, 19CT69, 19CT73, 19CT74, 19CT76, 19CT77, 19DT05, 19DT10, 19KT14, 19KT30, 19KT46, 19KT49, 19KT50, 19KT55, 19LT35, 20BT51, 20CT02, 20CT22, 20CT28, 20CT32, 20CT42, 20DT02, 20DT17, 20DT18, 20ET17, 20GG43, KME20H0750, KME20J2539, KME20J2680, KME20K0923, KME20K1114, KME20K1513, KME20K3034, KME20K3146, KME20L1867, KME20L2274, KME20M1511, KME21E0902, KME21F0741, KME21F1214, KME21F2006, KME21F2074, KME21K0095, KME21K1193, KME21K2275, KME21K2575, KME21K3015, KME21L0394, KME21L0799, KME21L1115, KME21L1276, KME21L1586, KME21M2500, KME21M2728, KME22A0787, KME22A2287, KME22A2957, KME22A2968, KME22B0519, KME22B1154, KME22B1696, KME22B1775, KME22B2179, KME22B2320, KME22B2477, KME22B2797, KME22C2074, KME22D1891, KME22D1892, KME22D3186, KME22D3488, KME22D3564, KME22E0663, KME22E0988, KME22E1279, KME22E1583, KME22E1811, KME22E2253

UPC codes

14026704341457

Source

Official record: FDA (Device enforcement)

Republished from the official source above; details can change — the source record controls.

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