Drug Recalls

Medtronic Vascular Recalls Angiographic Guidewire Component Due to Being Non-sterile

Posted on by Editor

Date: 07/02/2021

Product type:  Medical Device

Recalled Product

  • Angiographic Guidewire Component
  • Model Numbers:
    • WIRE ANGIO 107042 PNS .035X145 3MMJ PTFE; Part No: 107042
    • WIRE ANGIO 107044 PNS .038X145 3MMJ PTFE; Part No: 107044
    • WIRE ANGIO 107447 PNS .035X145 3MMJ PTFE; Part No: 107447
    • WIRE ANGIO 110003 PNS .035C145 3MMJ PTFE; Part No: 110003
    • WIRE ANGIO 110004 PNS.038X145 3MMJ LTPTF; Part No: 110004
  • Distribution Dates: November 23, 2007 to March 29, 2021
  • Devices Recalled in the U.S.: 54,997
  • Date Initiated by Firm: May 4, 2021

US-FDA Link: https://www.fda.gov/medical-devices/medical-device-recalls/medtronic-vascular-recalls-angiographic-guidewire-component-due-being-non-sterile