# FDA recall Z-0975-2022

> **Siemens Medical Solutions USA, Inc** · Class II · device recall initiated 2022-02-23.

## Product

Artis Q ceiling, Model Number 10848281

## Reason for recall

If the coolant level in the cooling circuit drops below a certain level, this may result in a situation in which the X-ray tube is no longer sufficiently cooled and the system will display the message "TUBE HOT, have a break". Several minutes later the system will block X-ray to prevent further damage and display the message "NO XRAY: TUBE TOO HOT".

## Distribution

US Nationwide.

## Key facts

- **Recall number:** Z-0975-2022
- **Recalling firm:** Siemens Medical Solutions USA, Inc
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2022-02-23
- **Report date:** 2022-04-27

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Malvern, PA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0975-2022

## Citation

> AI Analytics. FDA recall Z-0975-2022. Retrieved 2026-06-09 from https://api.ai-analytics.org/recall/Z-0975-2022. Source: US FDA. Licensed CC0.

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