# FDA recall Z-3214-2024

> **GE Healthcare** · Class II · device recall initiated 2024-08-05.

## Product

GE Healthcare Centricty PACS, V2, V3, V4, V6, V7; Radiological imaging processing system.

## Reason for recall

GE HealthCare has become aware of an issue where image storage is not possible when Centricity PACS reaches the maximum number of unique image identifiers (Ckeys). If this occurs, it can result in acquisition of a partial study.

## Distribution

Worldwide distribution.

## Key facts

- **Recall number:** Z-3214-2024
- **Recalling firm:** GE Healthcare
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2024-08-05
- **Report date:** 2024-10-02

- **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-3214-2024

## Citation

> AI Analytics. FDA recall Z-3214-2024. Retrieved 2026-07-20 from https://api.ai-analytics.org/recall/Z-3214-2024. Source: US FDA. Licensed CC0.

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