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The latest recall includes 686 devices in the U.S., distributed after the TurboHawk Plus received an FDA clearance in August 2021. (Medtronic) Medtronic and the FDA are expanding the reach of a Class ...
Medtronic has recalled the TurboHawk Plus directional atherectomy system, used in the peripheral arteries, due to the risk of catheter-tip damage during use, the US Food and Drug Administration ...
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 ...
Study Confirms Effectiveness of Directional Atherectomy with SilverHawk ™ and TurboHawk ™ Devices as a Frontline Therapy when Treating PAD LAS VEGAS--(BUSINESS WIRE)-- Covidien (NYSE:COV), a leading ...
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 ...
ラスベガス--(BUSINESS WIRE)--（ビジネスワイヤ）-- ヘルスケア製品世界的大手のコヴィディエン（NYSE:COV）は本日、 DEFINITIVE LE(Determination of Effectiveness of SilverHawk™ / TurboHawk™ Peripheral Plaque Excision ...
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