Tag: recall

Spectranetics' Bridge

FDA issues class I recall for Spectranetics’ Bridge occlusion balloon catheter

Spectranetics has recalled the Bridge occlusion catheter “due to the possibility of a blocked guidewire lumen in some device units”. Using affected catheters could...

Teleflex’s Vascular Solutions issues recall of Venture catheters

A worldwide recall of Venture catheters has been voluntarily initiated by its Teleflex’s Vascular Solutions subsidiary. Vascular Solutions, is the manufacturer of Venture catheters,...

US FDA designates Medtronic HVAD system controller field action as class...

The US Food and Drug Administration (FDA) has classified Medtronic’s recently initiated voluntary field action related to its HVAD system controllers and direct current...

US FDA issues Class I recall for 8040 Leonhard Lang multifunction...

The Leonhard Lang defibrillation electrode DF29N is being recalled due to a connector compatibility issue with the Welch Allyn AED model 10. The FDA...