Preformed AGT Oral Endotracheal Tube uncuffed/plain - Murphy, REF 100180035
FDA Recall #Z-1862-2023 — Class I — May 25, 2023
Product Description
Preformed AGT Oral Endotracheal Tube uncuffed/plain - Murphy, REF 100180035
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
4769 units
Distribution
US Nationwide distribution including Puerto Rico.
Code Information
UDI/DI 14026704340443, Batch Numbers: 18IG24, 18JG07, 18LG06, 18LG33, 19AG36, 19CT69, 19DT42, 19ET34, 19FT19, 19FT29, 19HT34, 19IT43, 19JT02, 19LT08, 19LT32, 20ET56, KME20K1811, KME20M0947, KME21A0060, KME21A2390, KME21B0599, KME22D1515, KME22G0175, KME22K0607, KME22K3167, KME23A1884
Status
Ongoing
Voluntary / Mandated
Voluntary: Firm initiated