---
title: "VANTAGE GALAN 3T. CMSC Model: MRT-3020/U7. Model Number: MEXL-3020/B7. — FDA record Z-0327-2026 | Is It on Recall"
description: "Affected system contains components that do not meet the required distance between electrodes for compliance with the IEC 60601-1 standard for medical electrica"
url: https://isitonrecall.com/recall/fda-device-z-0327-2026-vantage-galan-3t-cmsc-model-mrt-3020-u7-model-number-mexl-3020-b7/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

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

# VANTAGE GALAN 3T. CMSC Model: MRT-3020/U7. Model Number: MEXL-3020/B7. — FDA record Z-0327-2026

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 Oct 16, 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**: VANTAGE GALAN 3T. CMSC Model: MRT-3020/U7. Model Number: MEXL-3020/B7.
- **Reason**: Affected system contains components that do not meet the required distance between electrodes for compliance with the IEC 60601-1 standard for medical electrical equipment.
- **Classification**: Class II
- **Recalling firm**: Canon Medical System, USA, INC.
- **Quantity**: 2 units
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-0327-2026

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0327-2026%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 | CMSC Model: MRT-3020/U7. Model Number: MEXL-3020/B7. Serial Numbers: B7A2462002, B7A2522014. |

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

## Distribution

US distribution to Ohio and Nevada

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

- [Nevada](https://isitonrecall.com/state/nevada/)
- [Ohio](https://isitonrecall.com/state/ohio/)

## Dates in the source

- **Report date**: Nov 5, 2025
- **Recall initiation date**: Oct 16, 2025
- **Center classification date**: Oct 24, 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-0327-2026%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [Canon Medical System, USA, INC. records](https://isitonrecall.com/brand/canon-medical-system-usa-inc/)