# FDA recall Z-0242-2022

> **GE Healthcare, LLC** · Class II · device recall initiated 2021-06-30.

## Product

Computed Tomography Systems  Revolution CT,   Revolution CT ES,   Revolution Apex,   Revolution CT with Apex edition

## Reason for recall

The accumulated dose is incorrectly displayed in certain situations. Thisoccurs during an interventional exam using the SmartStep option if the table height is adjusted after  the exam starts. In this situation, the SmartStep display will show a value that is higher (up to 100  times) than the actual dose delivered.

## Distribution

Worldwide and US Nationwide Distribution

## Key facts

- **Recall number:** Z-0242-2022
- **Recalling firm:** GE Healthcare, LLC
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2021-06-30
- **Report date:** 2021-12-01

- **Voluntary/Mandated:** FDA Mandated
- **Location:** Waukesha, WI, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0242-2022

## Citation

> AI Analytics. FDA recall Z-0242-2022. Retrieved 2026-08-11 from https://api.ai-analytics.org/recall/Z-0242-2022. Source: US FDA. Licensed CC0.

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