Cordis Corporation: Medical Device Recall in 2020 - (Recall #: Z-1477-2020)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2020.

Data Source: FDA.

Product Description:

Cordis POWERFLEX P3, PTA Dilation Catheter, REF 420-6020S

Product Classification:

Class II

Date Initiated: January 8, 2020

Date Posted: March 18, 2020

Recall Number: Z-1477-2020

Event ID: 84680

Reason for Recall:

Cordis is recalling one (1) lot of POWERFLEX P3 PTA Dilatation Catheter due to the potential for body/shaft voids in the proximal seal area.

Status: Terminated

Product Quantity: 89 units

Code Information:

Lot 82155955, Use by date 2021-06-30

Distribution Pattern:

US and UK

Voluntary or Mandated:

Voluntary: Firm initiated