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

TELEFLEX LLC: Preformed AGT Oral Endotracheal Tube uncuffed/plain - Murphy, REF 100180050

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: 4146 units Lot/code info: UDI/DI 14026704340474, Batch Numbers: 18IG24, 18KG10, 18KG22, 18LG06, 18LG33, 19AG21, 19AG36, 19DT06, 19ET12, 19ET58, 19GT44, 19HT04, 19HT66, 19IT12, 19LT32, 20DT14, 20GG27, KME20J1208, KME21B0077, KME21C0441, KME22D3452, KME22F0736, KME22G0655

UPC codes

14026704340474

Source

Official record: FDA (Device enforcement)

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

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