HIGH

GE Healthcare Centricity Universal Viewer ZFP Recall 250 Units Worldwide in 2026

GE Healthcare recalled 250 Centricity Universal Viewer Zero Footprint Client units distributed worldwide after finding a risk that patient information may not match displayed images in certain workflows. The issue affects ZFP v6.0 SP11.6, SP11.6.0.1 and SP11.6.1 when Patient Timeline is installed. Hospitals should stop using affected units and await instructions from GE Healthcare.

Quick Facts at a Glance

Recall Date
January 16, 2026
Hazard Level
HIGH
Brand
GE Healthcare
Category
Health & Personal Care
Sold At
Unknown
Geographic Scope
1 states
At-Risk Groups
GENERAL

Hazard Information

Under certain workflows, patient information shown in the viewer may not match the images displayed on Centricity Universal Viewer Zero Footprint Client (ZFP) with versions ZFP v6.0: SP11.6, SP11.6.0.1 and SP11.6.1 on systems with Patient Timeline installed,

What You Should Do

Patients and healthcare providers should stop using this device immediately. Follow the recall instructions provided by the manufacturer. Contact GE Healthcare or your healthcare provider for instructions. Notification method: Letter

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Product Details

Model numbers: 2110344-039; 2110344-046; 2110344-047. Sold to healthcare facilities worldwide. When sold: not specified. Price: not specified.

The Hazard

The viewer may display patient information that does not correspond to the shown images in certain workflows on ZFP with the specified software versions and Patient Timeline installed.

Key Facts

  • 250 units recalled
  • Model numbers 2110344-039, 2110344-046, 2110344-047
  • Software versions affected: ZFP v6.0 SP11.6, SP11.6.0.1, SP11.6.1 with Patient Timeline
  • Distributed worldwide to healthcare facilities

Safety Guide

Not sure what to do next? Our guide walks you through the process step by step.

Read: What to Do When You Find a Recalled Product

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Safety Assessment

Risk LevelHIGH
Severity Score
8/ 10
Affected Groups
GENERAL
Injury Types
OTHER

Product Details

Model Numbers
2110344-039
2110344-046
2110344-047
Affected States
ALL
Report Date
March 11, 2026
Recall Status
ACTIVE

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