Preformed AGT Oral Endotracheal Tube uncuffed/plain - Murphy, REF 100180030
FDA Recall #Z-1861-2023 — Class I — May 25, 2023
Product Description
Preformed AGT Oral Endotracheal Tube uncuffed/plain - Murphy, REF 100180030
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
3100 units
Distribution
US Nationwide distribution including Puerto Rico.
Code Information
UDI/DI 14026704340436, Batch Numbers: 18GG26, 18GT26, 18JG14, 19AG21, 19CG07, 19CT69, 19DT42, 19ET34, 19FT29, 19HT04, 19IT43, 19KT17, 19LT08, 20DT15, 20DT24, 20ET56, KME20K1810, KME20M0946, KME20M2783, KME21A2389, KME21B0075, KME21B1923, KME22D1514, KME22F2666, KME22G0172, KME22G1751
Status
Ongoing
Voluntary / Mandated
Voluntary: Firm initiated