Medscape

Medtronic Recalls TurboHawk Directional Atherectomy System

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 ...
FierceBiotech

Medtronic, FDA expand HawkOne atherectomy recall to include TurboHawk Plus catheters

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 ...
MD&M East

Medtronic Recalls TurboHawk Due to HawkOne Recall

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 ...
TCTMD

Study Published in JACC CI Demonstrates Directional Atherectomy Effective as Frontline Therapy for Peripheral Arterial Disease Patients

Largest directional atherectomy study with independent, core lab analysis demonstrates high limb salvage in patients with critical limb ischemia and strong patency rates in both diabetic and ...