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

TELEFLEX LLC: Endotracheal Tube oral/nasal uncuffed/plain - Murphy, REF 100382050

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: 12382 units Lot/code info: UDI/DI 14026704340832, Batch Numbers: 18FG02, 18FT26, 18FT35, 18GG26, 18HT18, 18IG04, 18IG10, 18JG36, 18JT06, 18JT10, 18KG23, 18KT30, 18LG06, 18LT18, 19BG16, 19BG21, 19CG06, 19DT16, 19DT39, 19GT58, 19IT20, 19JT46, 19KT29, 19LT46, 20AT26, 20CT11, 20CT38, 20DT13, 20DT23, 20GG45, 20GT24, 20GT41, 20GT44, KME20H0293, KME20H1490, KME20H2049, KME20L1755, KME20L2383, KME20L2596, KME20M2056, KME21M2476, KME22A1524, KME22D0857, KME22D2479, KME22D3022, KME22F2427, KME22G0200, KME22G1191

UPC codes

14026704340832

Source

Official record: FDA (Device enforcement)

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

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