Skip to content

N/A 9730818Recalls & reported problems

Medtronic Navigation, Inc. · PROBE, 9730818 RIGHT 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 00721902984419), received between Mar 28, 2017 and Mar 28, 2017 — classified as 1 malfunction.

The most frequently reported specific device problem is “Imprecision” (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

  • Imprecision1

Patient problems

  • No Known Impact Or Consequence To Patient1

Recent adverse event reports

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

  • MalfunctionMar 28, 2017Imprecision; Imprecision

    A MEDTRONIC REPRESENTATIVE REPORTED THAT THE INSTRUMENT WAS CAUSING INACCURACIES DURING NAVIGATION. THERE WAS NO PATIENT IMPACT OR DELAY IN SURGERY REPORTED. SURGERY PROCEEDED AS PLANNED.

    Patient problems: No Known Impact Or Consequence To Patient

    MAUDE report 6440735 ↗

Other Orthopedic stereotaxic instrument devices

All Orthopedic stereotaxic instrument devices →

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