Endotracheal Tube oral/nasal uncuffed/plain - Murphy, REF 100382025
FDA Recall #Z-1934-2023 — Class I — May 25, 2023
Product Description
Endotracheal Tube oral/nasal uncuffed/plain - Murphy, REF 100382025
Reason for Recall
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.
Recalling Firm
TELEFLEX LLC — Morrisville, NC
Classification
Class I — Reasonable probability of serious adverse health consequences or death.
Product Type
Devices
Product Quantity
25630 units
Distribution
US Nationwide distribution including Puerto Rico.
Code Information
UDI/DI 14026704340788, Batch Numbers: 18FG22, 18FG31, 18FT13, 18GG16, 18GG34, 18GT12, 18HG08, 18IG13, 18IG14, 18JG09, 18JG14, 18JG35, 18KG08, 18LG15, 19AG04, 19AG07, 19AG21, 19BG12, 19CT37, 19CT41, 19CT44, 19CT64, 19ET57, 19FT25, 19GT04, 19GT29, 19KT65, 19LT03, 19LT27, 20AT37, 20BT15, 20CT12, 20DT04, 20ET03, 20ET33, 20FT21, 20FT40, 20GG41, KME20K2027, KME20K3208, KME21C1802, KME21C2684, KME21D0352, KME21D0601, KME21D1281, KME21D1818, KME21E1427, KME21M3077, KME22B1025, KME22B1089, KME22C0099, KME22E0297, KME22F0538, KME22F2559, KME22F2561, KME22G0176, KME22H1542, KME22K0062, KME22K0425, KME22K2437, KME22K2588, KME22L2985
Status
Ongoing
Voluntary / Mandated
Voluntary: Firm initiated