# FDA recall Z-0039-2025

> **GE Healthcare** · Class II · device recall initiated 2024-08-29.

## Product

GE Healthcare Centricity Universal Viewer Zero Footprint Client, Model/Catalog/Code Numbers:    a)¿¿¿¿¿ 2089507-120;   b)¿¿¿¿ 2089507-129;   c)¿¿¿¿¿ 2089507-131;   d)¿¿¿¿ 2089507-135;   e)¿¿¿¿ 2089507-136;   f)¿¿¿¿¿¿ 2089507-140;   g)¿¿¿¿¿ 2089507-144;   h)¿¿¿¿ 2089507-145;   i)¿¿¿¿¿¿ 2089507-149;   j)¿¿¿¿¿¿ 2089507-153;   k)¿¿¿¿¿ 2089507-154;   l)¿¿¿¿¿¿ 2089507-155;   m)¿¿¿ 2089507-156;   n)¿¿¿¿ 2089507-157;   o)¿¿¿¿ K2037DAED;   p)¿¿¿¿ K2037DBED;   q)¿¿¿¿ K2037DED;   r)¿¿¿¿¿ K2037DJED;   s)¿¿¿¿¿ K2037DNED;   t)¿¿¿¿¿ K2042TTED;   u)¿¿¿¿ K2049DC;   v)¿¿¿¿¿ K2049DD;   w)¿¿¿ K2049DF;   x)¿¿¿¿¿ P2037DAED;   y)¿¿¿¿¿ P2037DBED;   z)¿¿¿¿¿ P2037DED;   aa)¿¿ To be provided

## Reason for recall

GE HealthCare has become aware of an issue in Centricity Universal Viewer Zero Footprint Client (ZFP) version v6.0 SP11.x where the latest report is not shown by default to the user. The issue may occur when a study has multiple DICOM structured reports (i.e. preliminary, final, and/or addendum) stored in different series.

## Distribution

Worldwide distribution.

## Key facts

- **Recall number:** Z-0039-2025
- **Recalling firm:** GE Healthcare
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2024-08-29
- **Report date:** 2024-10-16

- **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-0039-2025

## Citation

> AI Analytics. FDA recall Z-0039-2025. Retrieved 2026-07-18 from https://api.ai-analytics.org/recall/Z-0039-2025. Source: US FDA. Licensed CC0.

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