---
title: "Ziehm Vision system, x-ray, tomography, computed. — FDA record Z-0575-2025 | Is It on Recall"
description: "Ziehm Imaging, Inc., distributor, have been informed by manufacturer, Ziehm Imaging GmbH that installed devices may not fully meet the requirements of IEC 60601"
url: https://isitonrecall.com/recall/fda-device-z-0575-2025-ziehm-vision-system-x-ray-tomography-computed/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

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

# Ziehm Vision system, x-ray, tomography, computed. — FDA record Z-0575-2025

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 Aug 8, 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**: Ziehm Vision system, x-ray, tomography, computed.
- **Reason**: Ziehm Imaging, Inc., distributor, have been informed by manufacturer, Ziehm Imaging GmbH that installed devices may not fully meet the requirements of IEC 60601-2-54 and or 21 CFR 1020.32(c) with respect to wired hand switch may fail when being exposed to mechanical stress such as shocks (e.g. dropping) or impacts can irreversibly damage the switching element in the hand switch. A defective switching element may then potentially initiate unintended radiation of the connected mobile X-ray unit.
- **Classification**: Class II
- **Recalling firm**: Orthoscan, Inc.
- **Quantity**: 3
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-0575-2025

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0575-2025%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: EZIEZIEHMVISIONFD1 Serial Numbers: 9246, 90155, 90416. |

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

## Distribution

U.S. (including Puerto Rico).

No US distribution state could be established from this record. Check the official notice.

## Dates in the source

- **Report date**: Dec 11, 2024
- **Recall initiation date**: Aug 8, 2024
- **Center classification date**: Dec 2, 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-0575-2025%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [Orthoscan, Inc. records](https://isitonrecall.com/brand/orthoscan-inc/)