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N/A 9734434Recalls & reported problems

Medtronic Navigation, Inc. · PROBE 9734434 LEFT 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 00763000121273), received between Jun 4, 2019 and Jun 4, 2019 — 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.

  • MalfunctionJun 4, 2019Material Integrity Problem; Material Integrity Problem

    MEDTRONIC RECEIVED INFORMATION REGARDING A LUMBAR PROBE OUTSIDE OF A PROCEDURE. IT WAS REPORTED THAT THE PROBE WAS DAMAGED. THERE WAS NO PATIENT PRESENT WHEN THIS ISSUE WAS IDENTIFIED. IT WAS NOT REPORTED IF THE INSTRUMENT WAS ABLE TO PASS VERIFICATION.

    Patient problems: No Patient Involvement

    MAUDE report 8667088 ↗

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