TELEFLEX LLC Recall 92373
Description: Endotracheal Tube oral/nasal Murphy Eye, High Volume, Low Pressure Cuff, REF 112082090
TELEFLEX LLC Recall 92373 Information
| Status | Ongoing |
| Mandated? | Voluntary: Firm initiated |
| Recall Number | Z-1892-2023 |
| Event ID | 92373 |
| Event Description | Endotracheal Tube oral/nasal Murphy Eye, High Volume, Low Pressure Cuff, REF 112082090 |
| Product Type | Devices |
| Distribution | US Nationwide distribution including Puerto Rico. |
| Quantity | 30423 units |
| Recall Reason | Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products. |
| Device Classification | 20230705 |
| Device Code Info | UDI/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 Date | 20230629 |
| Recall Initiation Date | 20230525 |
| Recalling Firm | TELEFLEX LLC |
| Initial Notification | Letter |
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