Preformed AGT Oral Endotracheal Tube uncuffed/plain - Murphy, REF 100181065
FDA Recall #Z-1924-2023 — Class I — May 25, 2023
Product Description
Preformed AGT Oral Endotracheal Tube uncuffed/plain - Murphy, REF 100181065
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
2980 units
Distribution
US Nationwide distribution including Puerto Rico.
Code Information
UDI/DI 14026704340597, Batch Numbers: 18FT35, 18GG25, 18JG35, 18KG21, 18LG18, 19AG25, 19CT33, 19ET69, 20BT02, 20CT11, KME22B1670, KME22E1010, KME22E1408, KME22H0137, KME22J0202, KME22K2262
Status
Ongoing
Voluntary / Mandated
Voluntary: Firm initiated