# FDA recall Z-1500-2023

> **GE Healthcare** · Class II · device recall initiated 2023-03-28.

## Product

Centricity PACS-IW with Universal Viewer, Model/Catalog Numbers:  a) 2066908-061, b) 2066908-077, c) 2066908-086, d) 2066908-111, e) 2066908-123, f) 2066908-136, g) 2066908-150; Radiological Image Processing System

## Reason for recall

GE HealthCare has become aware of an issue where information from two different patients can be mismatched when correcting patient or study information.

## Distribution

Worldwide Distribution

## Key facts

- **Recall number:** Z-1500-2023
- **Recalling firm:** GE Healthcare
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2023-03-28
- **Report date:** 2023-05-10

- **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-1500-2023

## Citation

> AI Analytics. FDA recall Z-1500-2023. Retrieved 2026-06-14 from https://api.ai-analytics.org/recall/Z-1500-2023. Source: US FDA. Licensed CC0.

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