Cordis US Corp: Medical Device Recall in 2023 - (Recall #: Z-0286-2024)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2023.

Data Source: FDA.

Product Description:

Cordis ANGIOGRAPHIC CATHETERIZATION SETS, INFINITI THRULEMEN, 5F, REF CO0208, cardiac catheter

Product Classification:

Class I

Date Initiated: September 26, 2023

Date Posted: November 15, 2023

Recall Number: Z-0286-2024

Event ID: 93174

Reason for Recall:

Non-sterile product labeled as sterile was distributed.

Status: Ongoing

Product Quantity: 30 devices

Code Information:

UDI/DI 10705032025935, Lot Number 18223410

Distribution Pattern:

US Distribution to: OK

Voluntary or Mandated:

Voluntary: Firm initiated