Arrow-Trerotola Percutaneous Thrombolytic Device (PTD)

Date: 22/12/2021

Product Names: Arrow-Trerotola Percutaneous Thrombolytic Device (PTD)
Model Number: See Recall Database Entry
Manufacturing Dates: January 1, 2020 to December 31, 2021
Distribution Dates: February 1, 2020 to December 31, 2021
Devices Recalled in the U.S.: 24,895
Date Initiated by Firm: December 22, 2021

US-FDA Link: https://www.fda.gov/medical-devices/medical-device-recalls/arrow-international-llc-subsidiary-teleflex-inc-recalls-arrow-trerotola-percutaneous-thrombolytic