Endotracheal Tube oral/nasal uncuffed/plain - Murphy, REF 100382060
FDA Recall #Z-1938-2023 — Class I — May 25, 2023
Product Description
Endotracheal Tube oral/nasal uncuffed/plain - Murphy, REF 100382060
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
5600 units
Distribution
US Nationwide distribution including Puerto Rico.
Code Information
UDI/DI 14026704340856, Batch Numbers: 18FG02, 18FG28, 18FT08, 18FT33, 18JG15, 18KG23, 18KG39, 20BT17, 20CT07, KME20H1758, KME20H2730, KME21D0828, KME21J0120, KME21J1583, KME22A2339, KME22B0949, KME22B1778, KME22C2310, KME22D1804, KME22F0417, KME22F0556, KME22F1739
Status
Ongoing
Voluntary / Mandated
Voluntary: Firm initiated