TELEFLEX LLC Recall 92373
Description: Endotracheal Tube oral/nasal uncuffed/plain - Murphy, REF 100382035
TELEFLEX LLC Recall 92373 Information
Status | Ongoing |
Mandated? | Voluntary: Firm initiated |
Recall Number | Z-1875-2023 |
Event ID | 92373 |
Event Description | Endotracheal Tube oral/nasal uncuffed/plain - Murphy, REF 100382035 |
Product Type | Devices |
Distribution | US Nationwide distribution including Puerto Rico. |
Quantity | 25435 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 14026704340801, Batch Numbers: 18GG15, 18GT32, 18IG13, 18KG24, 18KG33, 18KG34, 18LG01, 18LG03, 19CG05, 19CT36, 19CT72, 19DT13, 19KT20, 20AT05, 20AT50, 20BG19, 20BT43, 20DT01, 20DT04, 20DT24, 20ET30, 20FT21, 20FT43, 20FT58, 20FT68, 20GT22, KME20G0092, KME20K0870, KME20L1581, KME20L1894, KME20M3043, KME21B0039, KME21B1553, KME21C0891, KME21C0930, KME21C1580, KME21L2524, KME22B0933, KME22C2632, KME22C2804, KME22D1106, KME22D2022, KME22D2157, KME22D2462, KME22D2650, KME22D3220, KME22D3334, KME22E0292, KME22E0669, KME22E2685, KME22E2686, KME22F1707, KME22F2556, KME22H1215, KME22J2124, KME22K0712, KME22K0713, KME22K1577, KME22K2171, KME22K2382, KME22K2545, KME22L1846, KME22L2147, KME22L2341, KME22L2372, KME22L2411, KME22M1269, KME22M2426 |
Center Classification Date | 20230629 |
Recall Initiation Date | 20230525 |
Recalling Firm | TELEFLEX LLC |
Initial Notification | Letter |
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