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

TELEFLEX LLC: Preformed AGT Oral Endotracheal Tube Murphy Eye, High Volume, Low Pressure Cuff, REF 111780050

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: 19842 units Lot/code info: UDI/DI 14026704341068, Batch Numbers: 18FG12, 18FG24, 18GG03, 18GT26, 18HG24, 18IG24, 18JG07, 18KG34, 18LG11, 18LG31, 19AG09, 19AG11, 19AG21, 19AG36, 19CG07, 19CT36, 19DT06, 19FT18, 19GT44, 19JT01, 19KT37, 19LT04, 19LT32, 20AT09, 20BT53, 20CT24, 20DT24, 20ET50, 20ET56, 20FT36, 20FT58, KME20J1117, KME20M0952, KME21A0202, KME21A2486, KME21B0747, KME21C0326, KME22A1676, KME22B0553, KME22B1725, KME22C2818, KME22D0293, KME22D2681, KME22F0733, KME22G0349, KME22G3043, KME22H1792, KME22J2836, KME22K0470, KME22K0876, KME22M1319, KME22M1954, KME23A0157, KME23A1282, KME23A1422, KME23A1483, KME23A2002, KME23A2278, KME23B0506

UPC codes

14026704341068

Source

Official record: FDA (Device enforcement)

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

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