Preformed AGT Oral Endotracheal Tube uncuffed/plain - Murphy, REF 100181030
FDA Recall #Z-1870-2023 — Class I — May 25, 2023
Product Description
Preformed AGT Oral Endotracheal Tube uncuffed/plain - Murphy, REF 100181030
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
2874 units
Distribution
US Nationwide distribution including Puerto Rico.
Code Information
UDI/DI 14026704340528, Batch Numbers: 18GG23, 18HG17, 18HG21, 18IG17, 18LG18, 19AG25, 19BG19, 19BG32, 19GT16, 19IT53, 19LT21, KME22F2174, KME22G1753
Status
Ongoing
Voluntary / Mandated
Voluntary: Firm initiated