Database updated: 27 October 2026

Safety Information

Medsafe Online Recall Database

Detail of Recall

Type of Product:Device
Medsafe Reference:24676
Brand Name:Teleflex Medical - Endotracheal tube, SU
Model:
Affected:Multiple Lots
Software version:
Recalling Organisation:Teleflex Medical New Zealand
OFFICE 011, 110 CARLTON GORE ROAD
Newmarket
Auckland 1023
Contact Information:027 476 4009
Manufacturer:Teleflex Medical
Issue:The manufacturer has identified an issue where the15 mm Sheridan connector becomes disconnected from the Endotracheal tube. The immediate consequence for patients is disconnection from the breathing circuit, which may result in insufficient oxygenation, requiring medical intervention.
Recall action type:Alert
Recall action:Manufacturer to issue advice regarding use
Level of recall:Hospital/Pharmacy/Laboratory
Date Commenced:10/6/2019
Hide menus
Show menus
0 1 2 4 5 6 7 9 [ /