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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About This Product

The Centricity Universal Viewer Zero Footprint Client is radiology viewing software used to display medical images and patient data across systems. The product is deployed in hospitals worldwide as part of GE Healthcare's Centricity platform.

Why This Is Dangerous

Under certain workflows, patient information shown in the viewer may not match the images displayed. This mismatch can lead to misidentification or misinterpretation of patient data during imaging review.

Industry Context

This recall is not part of a broader industry pattern.

Real-World Impact

Hospitals may need to halt use of affected viewers until remediation. The mismatch could affect patient safety and workflow efficiency, and may require manual reconciliation of data.

Practical Guidance

How to identify if yours is affected

  1. Check model numbers: 2110344-039, 2110344-046, 2110344-047.
  2. Confirm ZFP version: v6.0 SP11.6, SP11.6.0.1 or SP11.6.1 with Patient Timeline installed.
  3. Look for UDI 00840682102988 on device label.
  4. Review System IDs listed in recall materials: ZFP-02312614, ZFP-22180897, ZFP-25199248, ZFP-22203146, ZFP-25188736, ZFP-00106869, ZFP-00106870, ZFP-01300798, ZFP-25222931, ZFP-25248683, ZFP-25248688, ZFP-25248690, ZFP-25248695, ZFP-25248713, ZFP-25248716, ZFP-26580437, ZFP-26694204.
  5. If Patient Timeline is not installed, this recall may not apply.

Where to find product info

Serial numbers and identifiers can be found on the device label, patient timeline documentation, or GE service portal.

What timeline to expect

The recall notice does not specify a remediation timeline. Hospitals will receive instructions by letter from GE Healthcare.

If the manufacturer is unresponsive

  • Document all communications with GE Healthcare.
  • File a report with the facility risk management or compliance office.
  • Consult the FDA recall portal for additional guidance.

How to prevent similar issues

  • Verify software updates and patches before deployment.
  • Maintain current patient data reconciliation protocols.
  • Prefer updated viewing software from GE or approved vendors with validated data integrity.

Documentation advice

Keep the recall letter, note device identifiers, and preserve all communications and responses from GE Healthcare.

Product Details

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

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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