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

TELEFLEX LLC: Preformed AGT Oral Endotracheal Tube uncuffed/plain - Murphy, REF 100180060

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: 2714 units Lot/code info: UDI/DI 14026704340498, Batch Numbers: 18KG08, 18LG33, 19AG21, 19BG12, 19ET12, 19FT19, 19HT34, 19IT12, 19IT43, 19LT32, 20AT49, 20DT15, 20GG27, KME20K1813, KME20L2063, KME20M1586, KME21A2393, KME21C3189, KME22D3370, KME22F2673

UPC codes

14026704340498

Source

Official record: FDA (Device enforcement)

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

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