---
title: "ANGIOGUARD RX / XP Emboli Capture Guidewire System, REF 601814RM — FDA record Z-1494-2023 | Is It on Recall"
description: "There is a potential for separation of the ANGIOGUARD RX / XP delivery system and capture sheath which include but are not limited to situations of an intra-pro"
url: https://isitonrecall.com/recall/fda-device-z-1494-2023-angioguard-rx-xp-emboli-capture-guidewire-system-ref-601814rm/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

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

# ANGIOGUARD RX / XP Emboli Capture Guidewire System, REF 601814RM — FDA record Z-1494-2023

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 24, 2023. 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**: ANGIOGUARD RX / XP Emboli Capture Guidewire System, REF 601814RM
- **Reason**: There is a potential for separation of the ANGIOGUARD RX / XP delivery system and capture sheath which include but are not limited to situations of an intra-procedural delay, unplanned percutaneous or surgical intervention, or stroke; while a replacement device is prepared.
- **Classification**: Class I
- **Recalling firm**: Cordis US Corp
- **Quantity**: 27 units
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-1494-2023

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1494-2023%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 | UDI/DI 20705032056738; Lot Numbers: 35265658, 35264211, 35264225, 35265647 |

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

## Distribution

Worldwide distribution.

No US distribution state could be established from this record. Check the official notice.

## Dates in the source

- **Report date**: May 17, 2023
- **Recall initiation date**: Mar 24, 2023
- **Center classification date**: May 11, 2023

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-1494-2023%22)

## Related records

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