Preformed AGT Oral Endotracheal Tube uncuffed/plain - Murphy, REF 100180045
FDA Recall #Z-1864-2023 — Class I — May 25, 2023
Product Description
Preformed AGT Oral Endotracheal Tube uncuffed/plain - Murphy, REF 100180045
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
4155 units
Distribution
US Nationwide distribution including Puerto Rico.
Code Information
UDI/DI 14026704340467, Batch Numbers: 18GT26, 18KG10, 18LG06, 19AG11, 19AG21, 19CT69, 19DT06, 19FT29, 19FT49, 19GT43, 19HT66, 19JT55, 19KT17, 19LT08, 19LT32, 20AT49, 20BT53, 20DT15, 20ET04, 20GG27, KME20H2636, KME20K1812, KME20K2573, KME21L2619, KME21M1773, KME22E2900, KME22G0347, KME22J3224, KME22K0489
Status
Ongoing
Voluntary / Mandated
Voluntary: Firm initiated