---
title: "MRI system: Vantage Elan, Model: MRT-2020 — FDA record Z-1249-2024 | Is It on Recall"
description: "For some MRI systems, it has been found that some of the maximum Spatial Field Gradient (SFG) values displayed in \"System Information\" of the operation window a"
url: https://isitonrecall.com/recall/fda-device-z-1249-2024-mri-system-vantage-elan-model-mrt-2020/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

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

# MRI system: Vantage Elan, Model: MRT-2020 — FDA record Z-1249-2024

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 Jan 29, 2024. 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**: MRI system: Vantage Elan, Model: MRT-2020
- **Reason**: For some MRI systems, it has been found that some of the maximum Spatial Field Gradient (SFG) values displayed in "System Information" of the operation window and some of the maximum SFG values described in the safety manual are lower than the correct values, which may cause a patient with an MR conditional device to feel some discomfort during the MR scan.
- **Classification**: Class II
- **Recalling firm**: Canon Medical System, USA, INC.
- **Quantity**: 1
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-1249-2024

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1249-2024%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: 04987670101632. Serial Number: S1F2052753 |

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

## Distribution

Worldwide - US Nationwide distribution including in the states of MD, IL, WV, CA, AZ, PR, CO, GA, PA, WA, UT, OK, KY, IA, IN, TN, CT, WI, OH, AL, MT, NM, TX, MO, MN, OR, ID, WY, NV, AR, FL, SD, MI, NY, NJ, KS, LA, NH, VT, MS, SC, ME and the country of DO.

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

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- [New York](https://isitonrecall.com/state/new-york/)
- [Ohio](https://isitonrecall.com/state/ohio/)
- [Oklahoma](https://isitonrecall.com/state/oklahoma/)
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- [West Virginia](https://isitonrecall.com/state/west-virginia/)
- [Wyoming](https://isitonrecall.com/state/wyoming/)

## Dates in the source

- **Report date**: Mar 13, 2024
- **Recall initiation date**: Jan 29, 2024
- **Center classification date**: Mar 4, 2024

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-1249-2024%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/)
