Medtronic Plc MDT has initiated a voluntary recall to customers related to the risk associated with tip damage caused by guidewire prolapse in its 6 French (6Fr) TurboHawk Plus Directional Atherectomy ...
Medtronic has recalled 686 TurboHawk Plus Directional Atherectomy Systems because there is a risk that the guidewire within the catheter may move downward or prolapse during use, which may damage the ...
Medtronic and the FDA are expanding the reach of a Class I recall handed down in January for the medtech giant’s catheter designed to clear out clogged arteries. The previous recall covered more than ...
Editor's note: In an earlier version of this story, TurboHawk was misspelled. MD+DI regrets the error. Earlier this year, Medtronic recalled its HawkOne Directional ...
The TurboHawk features a four angled super cutter blade that are designed to provide an efficient directional atherectomy tool for above the knee interventions including severally calcified lesions ...
Covidien Announces Final Results from Landmark DEFINITIVE LE Study in Patients with Peripheral Arter
LAS VEGAS--(BUSINESS WIRE)-- Covidien (NYS: COV) , a leading global provider of healthcare products, today announced final 12-month results from its DEFINITIVE LE (Determination of Effectiveness of ...
Please provide your email address to receive an email when new articles are posted on . Other tools for interventional cardiologists have come and gone, but atherectomy technology has persisted and — ...
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