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GE Healthcare Centricity Universal Viewer
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MEDICAL DEVICE RECALLMODERATE

GE Healthcare Centricity Universal Viewer

GE Healthcare is recalling Centricity Universal Viewer software due to a risk of patient information and image mismatch.

What to do

Contact your GE Healthcare representative or service provider for software updates and instructions on how to mitigate the display error.

Recalled
Listed
Updated
Recall No.
Z-1475-2026
Agency
FDA
Firm
GE Healthcare
Recall ID
98368
Status
ONGOING

Recall at a glance

Quantity recalled
250 units

Why it was recalled

GE Healthcare is recalling specific versions of the Centricity Universal Viewer Zero Footprint Client due to a software error that may cause a mismatch between patient information and the images displayed. This issue occurs on systems with the Patient Timeline feature installed. The recall is distributed nationwide.

Is mine affected?

Check the model, lot, or serial number on the device or its packaging. Yours is affected if it matches one below.

GE Healthcare Centricity Universal Viewer Zero Footprint Client, Model Numbers: 2110344-039, 2110344-046, 2110344-047; System, Image Processing, Radiological

UDI-DI
00840682102988, 02312614, 22180897, 25199248, 22203146, 25188736, 00106869, 00106870, 01300798, 25222931, 25248683, 25248688, 25248690, 25248695, 25248713, 25248716, 26608643, 26580437, 26694204, 26694229

Where it was sold

Distributed nationwide.

Timeline

  1. Firm initiated recall
  2. Publicly announced
  3. Listed on Recall Canary
  4. Summary updated

Official source

View on U.S. Food and Drug Administration →

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Editorial summary by Recall Canary · summary updated 2026-06-11 · primary source: U.S. Food and Drug Administration · severity reflects the agency's published classification