# FDA recall Z-1489-2023

> **Cordis US Corp** · Class I · device recall initiated 2023-03-24.

## Product

ANGIOGUARD RX / XP Emboli Capture Guidewire System, REF 501814REC

## Reason for recall

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.

## Distribution

Worldwide distribution.

## Key facts

- **Recall number:** Z-1489-2023
- **Recalling firm:** Cordis US Corp
- **Classification:** Class I
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2023-03-24
- **Report date:** 2023-05-17

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Miami Lakes, FL, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1489-2023

## Citation

> AI Analytics. FDA recall Z-1489-2023. Retrieved 2026-06-25 from https://api.ai-analytics.org/recall/Z-1489-2023. Source: US FDA. Licensed CC0.

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