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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 111781080

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: 8620 units Lot/code info: UDI/DI 14026704341242, Batch Numbers: 18GG18, 18HG21, 18IG16, 18KG01, 18KG19, 18LG18, 19BG18, 19BG33, 19GT13, 19HT31, 19HT55, 19IT15, 19JT35, 19KT14, 19LT21, 20AT26, 20CT11, 20FT68, 20GT49, KME20M0409, KME21A1111, KME21A2095, KME21B2212, KME21C2483, KME21C3405, KME22B0921, KME22B0923, KME22D0289, KME22D1811, KME22D1855, KME22D2401, KME22E2898, KME22H2600, KME22H3295, KME22J2877, KME22K2861, KME22K3117, KME22M1510, KME22M2546, KME23B0521, KME23B3047

UPC codes

14026704341242

Source

Official record: FDA (Device enforcement)

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

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