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N/A 9734433Recalls & reported problems

Medtronic Navigation, Inc. · PROBE 9734433 RIGHT LUMBAR TACTILE · 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 00763000050832), received between Feb 5, 2020 and Feb 5, 2020 — classified as 1 malfunction.

The most frequently reported specific device problem is “Material Integrity 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. How this data works · Data updated Oct 13, 2026.

Most reported problems

Device problems

  • Material Integrity Problem1

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.

  • MalfunctionFeb 5, 2020Material Integrity Problem; Material Integrity Problem

    MEDTRONIC RECEIVED INFORMATION REGARDING A NAVIGATION SYSTEM. IT WAS REPORTED OUTSIDE OF A PROCEDURE THAT THE PROBE TIP HAD BEEN BENT AND IT WAS VISIBLY NOTICEABLE. NO PATIENT WAS PRESENT AT THE TIME OF THE EVENT. ADDITIONAL INFORMATION WAS RECEIVED STATING THAT THE INSTRUMENT WAS BELIEVED TO BE ABLE TO PASS VERIFICATION. BUT IT WAS CLEARLY BENT.

    Patient problems: No Patient Involvement

    MAUDE report 9671872 ↗

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