Cordis Recalls SUPER TORQUE MB Angiographic Catheter with Radiopaque Marker Bands Due to Potential for Marker Bands to Move or Dislodge

Date: 09/22/2021

Product type: Medical Device

Recalled Product

• Cordis SUPER TORQUE MB Angiographic Catheter with Radiopaque Marker Bands
• Lot Numbers: See Database Entry
• Distribution Dates: January 1, 2019 to July 20, 2021
• Devices Recalled in the U.S.: 25,000 units
• Date Initiated by Firm: May 19, 2021

US-FDA Link: https://www.fda.gov/medical-devices/medical-device-recalls/cordis-recalls-super-torque-mb-angiographic-catheter-radiopaque-marker-bands-due-potential-marker