# FDA recall Z-0143-2024

> **GE Healthcare** · Class II · device recall initiated 2023-09-08.

## Product

Universal Viewer Workflow Manager, Image processing radiological system

## Reason for recall

When using Universal Viewer or Centricity Universal Viewer with Workflow Manager (WFM), if a third-party reporting application is used to launch exams, it could display information on a different patient than WFM and the Viewer.

## Distribution

Nationwide distribution to AR, AZ, CA, CO, DE, FL, GA, IL, IN, ME, MI, MN, MO, NE, NJ, NM, NV, NY, OH, OK, PA, SC, SD, TN, TX.    International distribution to Austria, Canada, France, Germany, Hong Kong, Israel, Italy, Philippines, Singapore, Thailand, Turkey, Vietnam.

## Key facts

- **Recall number:** Z-0143-2024
- **Recalling firm:** GE Healthcare
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2023-09-08
- **Report date:** 2023-11-01

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Chicago, IL, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0143-2024

## Citation

> AI Analytics. FDA recall Z-0143-2024. Retrieved 2026-07-13 from https://api.ai-analytics.org/recall/Z-0143-2024. Source: US FDA. Licensed CC0.

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