# FDA recall Z-1466-2022

> **GE Healthcare, LLC** · Class II · device recall initiated 2022-06-14.

## Product

Centricity PACS Software Version 7.0 SP0.0.4.7

## Reason for recall

The Event Notification Manager (ENM) functionality for certain products does not process notifications for study modifications performed on post verified exams.

## Distribution

Worldwide distribution - US Nationwide distribution in the states of CO, NV, OH, PA, WA and the countries of Brazil, Canada, China, France, Germany, Israel, Italy, Japan, Oman, Spain, Switzerland, and United Kingdom.

## Key facts

- **Recall number:** Z-1466-2022
- **Recalling firm:** GE Healthcare, LLC
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2022-06-14
- **Report date:** 2022-08-03
- **Termination date:** 2024-01-16

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

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1466-2022

## Citation

> AI Analytics. FDA recall Z-1466-2022. Retrieved 2026-07-09 from https://api.ai-analytics.org/recall/Z-1466-2022. Source: US FDA. Licensed CC0.

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