The US Food and Drug Administration has issued a Class I recall for the Arrow International intra-aortic balloon catheter and percutaneous insertion kits made by Teleflex Incorporated. The reason for ...

Please provide your email address to receive an email when new articles are posted on . The recall of two varieties of intra-aortic balloon catheter kits has been ...

Struggling Teleflex ($TFX) in February warned of an impending restructuring plan that will involve the usual mix of layoffs, relocations and outsourcing. The Wayne ...

The Cardiosave Hybrid and Cardiosave Rescue intra-aortic balloon pumps (IABPs) have been hit with another recall by the manufacturer (Getinge/Datascope), this time due to damage to the balloon ...

Major adverse cardiac and CV events were not reduced in patients with severe left ventricular dysfunction and extensive coronary disease who had an intra-aortic balloon inserted before percutaneous ...

One way of assessing or assigning risk is to use a 'myocardium at risk' score. These scores help to systematically calculate the severity of CAD based on angiographic findings and also give an ...

WAYNE, Pa.--(BUSINESS WIRE)--Teleflex Incorporated (NYSE: TFX), a leading global provider of medical technologies for critical care, urology and surgery, coronary and peripheral interventions, will ...

Less invasive catheter-based aortic valve replacement and open valve-replacement surgery have a similar one-year survival for patients at high risk for surgery, according to a recent study. Less ...

The applicability and validity of registry data remains open to debate. When studying a patient cohort that is notoriously difficult to enroll in randomized trials, registry data can certainly add ...