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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 ...

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 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 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 ...