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PROBE DRIVING UNIT MAJ-1720 (UDI 04953170311192)Recalls & reported problems

Olympus Medical Systems Corp. · Class 2

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 04953170311192), received between Nov 19, 2020 and Nov 19, 2020 — classified as 1 malfunction.

The most frequently reported specific device problem is “Failure to Power Up” (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. How this data works · Data updated Oct 13, 2026.

Most reported problems

Device problems

  • Failure to Power Up1

Patient problems

  • No Patient Involvement1

Recent adverse event reports

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

  • MalfunctionNov 19, 2020Failure to Power Up; Failure to Power Up

    IT IS REPORTED WHILE PREPARING FOR AN UNSPECIFIED PROCEDURE USING A PROBE DRIVING UNIT, THE UNIT WOULD NOT TURN ON. THE DEVICE WAS INSPECTED AND NO DAMAGE OR ABNORMALITIES WERE NOTED. THERE WAS NO PATIENT INJURY RELATED TO THIS EVENT.

    Patient problems: No Patient Involvement

    MAUDE report 10868303 ↗

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