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NIM-ECLIPSE® NCCPU (UDI 00643169468573)Recalls & reported problems

Medtronic Xomed, Inc. · COMPUTER NCCPU NOTEBOOK E6540 ROHS · Class 2

All models of NIM-ECLIPSE (7)

Data updated Oct 16, 2026 from official FDA records · Editorial policy

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

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00643169468573), received between Oct 6, 2021 and Oct 6, 2021 — classified as 1 malfunction.

The most frequently reported specific device problem is “Connection Problem” (1 report).

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. What reports can and can't tell you · How this data works · Data updated Oct 16, 2026.

Most reported problems

Device problems

  • Connection Problem1
  • Display or Visual Feedback Problem1
  • Use of Device Problem1

Patient problems

  • No Clinical Signs, Symptoms or Conditions1

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

  • MalfunctionOct 6, 2021Display or Visual Feedback Problem; Use of Device Problem; Connection Problem; Display or Visual Feedback Problem; Use of Device Problem; Connection Problem

    ON FOLLOW-UP, IT WAS REPORTED THAT THE COMPUTER HAD A MESSAGE: "THE COMPUTER NOT CONNECTED TO CONTROLLER" PRIOR TO USE. FOR TROUBLESHOOTING, THEY TRIED TO CONNECT WITH OTHER CABLE, BUT THE CONTROLLER WAS NOT RECOGNIZED BY THE COMPUTER.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 12583426 ↗

Other STIMULATOR, ELECTRICAL, EVOKED RESPONSE devices

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Sources and updates

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