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MUSE NXRecalls & reported problems

GE Medical Systems Information Technologies, Inc. · MUSE NX · Class 2

Data updated Oct 13, 2026 from official FDA records · Editorial policy

Adverse event reports
0
Deaths reported
0
Injuries reported
0
Recalls naming it
1

Summary

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

1 FDA recall record name this device's identifier.

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. Mar 16, 2022Terminated

    Two scenarios may cause edits to measurements and diagnosis statements can be lost after a test is Signed in the MUSE NX web client.

    Z-0919-2022 · Root cause: Software Manufacturing/Software Deployment · FDA record ↗

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Sources and updates

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