Cordis Corporation: Medical Device Recall in 2019 - (Recall #: Z-0250-2020)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2019.

Data Source: FDA.

Product Description:

Cordis MAXI LD PTA Dilatation Catheter, for cardiovascular use.

Product Classification:

Class II

Date Initiated: October 4, 2019

Date Posted: November 6, 2019

Recall Number: Z-0250-2020

Event ID: 83977

Reason for Recall:

Product was manufactured utilizing an expired inner body.

Status: Terminated

Product Quantity: 21 units

Code Information:

Catalog Number: 4171460S; Lot Number: 82169860; Expiry Date: 10/31/2020

Distribution Pattern:

US distribution to AL, AZ, FL, MN, and MO

Voluntary or Mandated:

Voluntary: Firm initiated