Preformed AGT Oral Endotracheal Tube uncuffed/plain - Murphy, REF 100180040
FDA Recall #Z-1863-2023 — Class I — May 25, 2023
Product Description
Preformed AGT Oral Endotracheal Tube uncuffed/plain - Murphy, REF 100180040
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
5120 units
Distribution
US Nationwide distribution including Puerto Rico.
Code Information
UDI/DI 14026704340450, Batch Numbers: 18GT26, 18KG10, 18LG33, 19AG21, 19BG12, 19CT36, 19DT42, 19FT29, 19FT49, 20DT24, KME20L2493, KME20M0278, KME21A0061, KME21B1925, KME21M1736, KME22C0700, KME22F0734, KME22G0184, KME22H0033, KME22H3078, KME22J0843
Status
Ongoing
Voluntary / Mandated
Voluntary: Firm initiated