Cordis US Corp: Medical Device Recall in 2025 - (Recall #: Z-1510-2025)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2025.

Data Source: FDA.

Product Description:

Cordis, REF C10040ML, Smart Control Vascular Stent System ILIAC, 10mm X 40mm 6F, SterileEO, Rx Only

Product Classification:

Class II

Date Initiated: March 4, 2025

Date Posted: April 9, 2025

Recall Number: Z-1510-2025

Event ID: 96418

Reason for Recall:

product mix-up; Vascular stent labeled as one size but contains a different size.

Status: Ongoing

Product Quantity: 20 units

Code Information:

Lot: 18298569/UDI: (01)20705032024591

Distribution Pattern:

US Distribution to states of: AR, AZ, FL, NJ, TN; and OUS Foreign country of: Japan

Voluntary or Mandated:

Voluntary: Firm initiated