# FDA recall Z-3160-2024

> **GE Healthcare** · Class II · device recall initiated 2024-07-23.

## Product

GE Healthcare Centricity Universal Viewer Zero Footprint Client,  Model Numbers:    a) 2110344-008;   b) 2110344-009;   c) 2110344-010;   d) 2110344-011;   e) 2110344-013;   f) 2110344-019;   g) 2110344-025;   h) 2110344-029;   i) 2110344-030;   j) 2110344-032    ; Radiological image processing system

## Reason for recall

Footprint Client (ZFP) versions v6.0 SP9.x and SP10.x where the latest addended report is not shown by default to the user. The issue occurs when the addendum is created on the same day as the original report but at a different time, and only when launched on the following browsers.  " Internet Explorer 10 (IE10)  " Internet Explorer 11 (IE11)  " Firefox.

## Distribution

Worldwide distribution.

## Key facts

- **Recall number:** Z-3160-2024
- **Recalling firm:** GE Healthcare
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2024-07-23
- **Report date:** 2024-09-25

- **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-3160-2024

## Citation

> AI Analytics. FDA recall Z-3160-2024. Retrieved 2026-07-01 from https://api.ai-analytics.org/recall/Z-3160-2024. Source: US FDA. Licensed CC0.

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