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Universal Viewer 8Recalls & reported problems

Ge Healthcare · MD UV 8 MEDICAL DEVICE · Class 2

2 open recalls name this device. See the recall details and contact the manufacturer or your healthcare provider.

Adverse event reports
0
Deaths reported
0
Injuries reported
0
Recalls naming it
2

Summary

No MAUDE adverse event reports in our data reference this device identifier directly.

2 FDA recall records name this device's identifier, 2 still open.

Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. How this data works · Data updated Oct 13, 2026.

Recalls naming this device

  1. Sep 8, 2023Open, Classified

    When using Universal Viewer or Centricity Universal Viewer with Workflow Manager (WFM), if a third-party reporting application is used to launch exams, it could display information on a different patient than WFM and the Viewer.

    Z-0143-2024 · Root cause: Software design · FDA record ↗

  2. Jul 15, 2022Open, Classified

    Inaccurate Distance and Area measurements with use of Global Stack viewport.

    Z-1566-2022 · Root cause: Process design · FDA record ↗

Other System, image processing, radiological devices

All System, image processing, radiological devices →

Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.