Medtronic Recalls TurboHawk Plus Directional Atherectomy System Due to Risk of Tip Damage During Use

Date:  03/09/2022

Product type: Medical Devices

• Product Names: TurboHawk Plus Directional Atherectomy System

Product Codes: 

• See Recall Database Entry (Small vessel)
• See Recall Database Entry (Multi vessel)

• Manufacturing Dates: July 21, 2021 to November 25, 2021
• Distribution Dates: September 27, 2021 to January 25, 2022
• Devices Recalled in the U.S.: 686
• Date Initiated by Firm: February 4, 2022

USA-FDA Link:  https://www.fda.gov/medical-devices/medical-device-recalls/medtronic-recalls-turbohawk-plus-directional-atherectomy-system-due-risk-tip-damage-during-use