TELEFLEX LLC Recall 92373
Description: Endotracheal Tube oral/nasal uncuffed/plain - Murphy, REF 100382055
TELEFLEX LLC Recall 92373 Information
Status | Ongoing |
Mandated? | Voluntary: Firm initiated |
Recall Number | Z-1937-2023 |
Event ID | 92373 |
Event Description | Endotracheal Tube oral/nasal uncuffed/plain - Murphy, REF 100382055 |
Product Type | Devices |
Distribution | US Nationwide distribution including Puerto Rico. |
Quantity | 7800 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 14026704340849, Batch Numbers: 18FG21, 18FG33, 18FT17, 18FT31, 18GT06, 18HG06, 18HG15, 18IT06, 18JG14, 18JT12, 18KG10, 19AG05, 19AT23, 19BG10, 19BG21, 19BG26, 19BT08, 20CT47, 20DT01, 20GG45, 20GT40, KME20H0294, KME20H3036, KME20J0600, KME20J2166, KME20K1116, KME20K1206, KME20K3277, KME20L1040, KME20L1224, KME22F2548 |
Center Classification Date | 20230629 |
Recall Initiation Date | 20230525 |
Recalling Firm | TELEFLEX LLC |
Initial Notification | Letter |
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