Cordis Corporation: Medical Device Recall in 2021 - (Recall #: Z-2428-2021)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2021.

Data Source: FDA.

Product Description:

Cordis 5F UNIVERSAL FLUSH F4 SUPER TORQUE MB, SPECIAL, Angiographic Catheter, REF SRD6785MB

Product Classification:

Class I

Date Initiated: July 21, 2021

Date Posted: September 22, 2021

Recall Number: Z-2428-2021

Event ID: 88372

Reason for Recall:

Cordis has identified that the SUPER TORQUE MB Angiographic Catheter (with Marker Bands) are being used in a manner that may allow entrapment of the catheter between endovascular devices and the vessel wall, which can lead to marker band movement or dislodgement.

Status: Terminated

Product Quantity: 45 units

Code Information:

All codes

Distribution Pattern:

Worldwide distribution - US Nationwide distribution and the countries of Canada, Europe.

Voluntary or Mandated:

Voluntary: Firm initiated