---
title: "Vista Brite Tip, Judkins Right 4, REF SM7504, JR3 VBT (Special) 110 cm 6F. Gu... — FDA record Z-1330-2025 | Is It on Recall"
description: "Catheter manufactured at the incorrect length."
url: https://isitonrecall.com/recall/fda-device-z-1330-2025-vista-brite-tip-judkins-right-4-ref-sm7504-jr3-vbt-special-110-cm-6f-guiding-catheter-is-intended-fo/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

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

# Vista Brite Tip, Judkins Right 4, REF SM7504, JR3 VBT (Special) 110 cm 6F. Guiding catheter is intended for use for i... — FDA record Z-1330-2025

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 Feb 7, 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**: 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**: Catheter manufactured at the incorrect length.
- **Classification**: Class II
- **Recalling firm**: Cordis US Corp
- **Quantity**: 12 units
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-1330-2025

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1330-2025%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 | UDI: 20705032042991/ Lot Number: 18368326 |

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

## Distribution

US: WA OUS: Japan

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

- [Washington](https://isitonrecall.com/state/washington/)

## Dates in the source

- **Report date**: Mar 19, 2025
- **Recall initiation date**: Feb 7, 2025
- **Center classification date**: Mar 13, 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-1330-2025%22)

## Related records

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