Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.
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: 15020 Lot/code info: UDI/ID 4026704319565, Batch numbers: 18FG05, 18FG25, 18GG05, 18GG10, 18GG20, 18GT32, 18HG19, 18HG32, 18HG38, 18IG09, 18JG04, 18JG06, 18JG34, 18KG35, 19AG13, 19AG37, 19BG01, 19CT58, 19CT71, 19DT15, 19ET60, 19FT41, 19GT38, 19HT15, 19HT61, 19HT66, 19IT25, 19JT18, 19JT22, 19JT57, 19JT70, 19KT41, 20AT25, 20AT53, 20BT27, 20CT05, 20CT22, 20DT37, 20ET21, 20GT14, KME20H0903, KME20H0904, KME20H2018, KME20J1239, KME20J1240, KME20K0938, KME20K2623, KME20L0487, KME20L1705, KME20M1578, KME20M1751, KME21K1127, KME21K1256, KME21K3029
4026704319565
Official record: FDA (Device enforcement) ↗
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