Home » MHRA Issues Medical Device Alert for Endotracheal Tube
MHRA Issues Medical Device Alert for Endotracheal Tube
The Medicines and Healthcare products Regulatory Agency (MHRA) has issued an alert for Teleflex’s Rüsch Flexislip/Flexi-Slip endotracheal tube stylet with soft distal tip, 6F. The company has received two complaints regarding the tube: for difficulty removing the stylet from the endotracheal tube after intubation and for a separation of the PVC sheath from the stylet.
Upcoming Events
-
25Apr
-
07May
-
14May
-
30May