# FDA recall Z-1330-2025

> **Cordis US Corp** · Class II · device recall initiated 2025-02-07.

## Product

Vista Brite Tip, Judkins Right 4, REF SM7504, JR3 VBT (Special) 110 cm 6F.  Guiding catheter is intended for use for intravascular introduction of interventional/diagnostic devices into the coronary or peripheral vascular systems.

## Reason for recall

Catheter manufactured at the incorrect length.

## Distribution

US: WA OUS: Japan

## Key facts

- **Recall number:** Z-1330-2025
- **Recalling firm:** Cordis US Corp
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2025-02-07
- **Report date:** 2025-03-19

- **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-1330-2025

## Citation

> AI Analytics. FDA recall Z-1330-2025. Retrieved 2026-07-01 from https://api.ai-analytics.org/recall/Z-1330-2025. Source: US FDA. Licensed CC0.

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