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TELEFLEX LLC Recall 92373

Description: Endotracheal Tube oral/nasal Murphy Eye, High Volume, Low Pressure Cuff, REF 112082090

TELEFLEX LLC Recall 92373 Information

Mandated?Voluntary: Firm initiated
Recall NumberZ-1892-2023
Event ID92373
Event DescriptionEndotracheal Tube oral/nasal Murphy Eye, High Volume, Low Pressure Cuff, REF 112082090
Product TypeDevices
DistributionUS Nationwide distribution including Puerto Rico.
Quantity30423 units
Recall ReasonReports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.
Device Classification20230705
Device Code InfoUDI/DI 14026704341464, Batch Numbers: 18FG23, 18FT17, 18FT24, 18FT25, 18FT49, 18GG12, 18GG26, 18JG38, 18KG04, 18KG05, 18KG23, 18KG26, 18KG38, 18KT04, 18KT27, 18LG13, 19AT19, 19CG02, 19ET11, 19JT61, 19KT35, 19LT35, 19LT46, 20AT57, 20BT38, 20DT28, KME20H0415, KME20H2140, KME20H2314, KME20H2913, KME20J1999, KME20K0212, KME20K0600, KME20K1434, KME20K3525, KME20L0805, KME21K0478, KME21L1274, KME21L1371, KME22A2199, KME22A2286, KME22A2317, KME22B1140, KME22B1997, KME22B2180, KME22C0133, KME22C0202, KME22C0454, KME22C0573, KME22C0675, KME22D3492, KME22E1281, KME22E1282, KME22E2749, KME22F2444, KME22H2380, KME22K0996, KME23A2734, KME23B2546
Center Classification Date20230629
Recall Initiation Date20230525
Recalling FirmTELEFLEX LLC
Initial Notification Letter
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