Arrow International, LLC (Subsidiary of Teleflex Inc.) Recalls the Arrow-Trerotola Percutaneous Thrombolytic Device Due to Risk of Tip Damage During Use

Date: 02/23/2022

Product type: Medical Devices

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

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