---
title: "Cordis, REF C10040ML, Smart Control Vascular Stent System ILIAC, 10mm X 40mm ... — FDA record Z-1510-2025 | Is It on Recall"
description: "product mix-up; Vascular stent labeled as one size but contains a different size."
url: https://isitonrecall.com/recall/fda-device-z-1510-2025-cordis-ref-c10040ml-smart-control-vascular-stent-system-iliac-10mm-x-40mm-6f-sterileeo-rx-only/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

[Recall archive](https://isitonrecall.com/archives/) / FDA device enforcement

# Cordis, REF C10040ML, Smart Control Vascular Stent System ILIAC, 10mm X 40mm 6F, SterileEO, Rx Only — FDA record Z-1510-2025

Reported ongoing

Status as reported in the agency record. FDA warns that enforcement status may not track the current recall lifecycle; check the current official notice.

Source date Mar 4, 2025. Retrieved Oct 1, 2026. Last updated Oct 1, 2026.

Archive changed Oct 1, 2026. USDA FSIS records are unavailable; [check FSIS directly](https://www.fsis.usda.gov/recalls). [Source coverage and dates](https://isitonrecall.com/sources/).

## What the record says

- **Product**: Cordis, REF C10040ML, Smart Control Vascular Stent System ILIAC, 10mm X 40mm 6F, SterileEO, Rx Only
- **Reason**: product mix-up; Vascular stent labeled as one size but contains a different size.
- **Classification**: Class II
- **Recalling firm**: Cordis US Corp
- **Quantity**: 20 units
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-1510-2025

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1510-2025%22)

[What the recall classes mean](https://isitonrecall.com/guides/recall-classes/). Classification is an agency assessment, not individual medical advice.

## Lot and product identifiers

| Label field | Details supplied by the agency |
| --- | --- |
| Lot, code or applicability | Lot: 18298569/UDI: (01)20705032024591 |

Match all identifying details in the current notice. A brand name alone is not enough.

## Distribution

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

States below are derived from the distribution text, including nationwide wording. They are not inferred from the firm's address.

- [Arkansas](https://isitonrecall.com/state/arkansas/)
- [Arizona](https://isitonrecall.com/state/arizona/)
- [Florida](https://isitonrecall.com/state/florida/)
- [New Jersey](https://isitonrecall.com/state/new-jersey/)
- [Tennessee](https://isitonrecall.com/state/tennessee/)

## Dates in the source

- **Report date**: Apr 9, 2025
- **Recall initiation date**: Mar 4, 2025
- **Center classification date**: Apr 3, 2025

FDA company pages use the listing date; enforcement records use initiation dates; CPSC uses recall date; NHTSA uses report-received date. These dates are not interchangeable.

## What to do next

Read the official notice for the action that applies to your exact product.

[Read the current instructions](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1510-2025%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [Cordis US Corp records](https://isitonrecall.com/brand/cordis-us-corp/)