Date: 01/21/2022

Product type:  Null

  • HawkOne Directional Atherectomy System
  • Product Codes and Lot Numbers: See Recall Database Entry
  • Devices Recalled in the United States: 95,110
  • Distribution Date: January 22, 2018 to October 4, 2021
  • Date Initiated by Firm: December 6, 2021

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