Date: 04/02/2022
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