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Wednesday, March 9, 2022
US FDA News: Medtronic Recalls TurboHawk Plus Directional Atherectomy System Due to Risk of Tip Damage During Use
This device is used during an atherectomy to treat patients who have calcified narrowings and blockages in the peripheral arteries.
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Medtronic Recalls TurboHawk Plus Directional Atherectomy System Due to Risk of Tip Damage During Use
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