Teleflex Incorporated Announces Worldwide Recall of Arrow-Trerotola™ Over-The-Wire PTD® Kit Percutaneous Thrombolytic Device: 7FR

Date: 11/30/2021

Product type: Medical Devices, Unapproved Use

Company Announcement Date: November 26, 2021
FDA Publish Date: November 30, 2021
Product Type: Medical Devices
Reason for Announcement: Inner lumen may detach from the device’s basket
Company Name: Teleflex Incorporated
Brand Name: Arrow
Product Description: Arrow-Trerotola™ Over-The-Wire PTD® Kit Percutaneous Thrombolytic Device: 7FR

US-FDA Link: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/teleflex-incorporated-announces-worldwide-recall-arrow-trerotolatm-over-wire-ptdr-kit-percutaneous