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

TELEFLEX LLC: Preformed AGT Oral Endotracheal Tube uncuffed/plain - Murphy, REF 100180035

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: 4769 units Lot/code info: UDI/DI 14026704340443, Batch Numbers: 18IG24, 18JG07, 18LG06, 18LG33, 19AG36, 19CT69, 19DT42, 19ET34, 19FT19, 19FT29, 19HT34, 19IT43, 19JT02, 19LT08, 19LT32, 20ET56, KME20K1811, KME20M0947, KME21A0060, KME21A2390, KME21B0599, KME22D1515, KME22G0175, KME22K0607, KME22K3167, KME23A1884

UPC codes

14026704340443

Source

Official record: FDA (Device enforcement)

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

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