Skip to content

StealthStation Cranial Software 9735762 (UDI 00763000125295)Recalls & reported problems

Medtronic Navigation, Inc. · SFW 9735762 APP STEALTH S8 APPLICATION · Class 2

All models of StealthStation Cranial Software (5)

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

1 open recall names this device. See the recall details and contact the manufacturer or your healthcare provider.

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

Summary

No MAUDE adverse event reports in our data reference this device identifier directly.

1 FDA recall record name this device's identifier, 1 still open.

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.

Recalls naming this device

  1. Mar 26, 2024Open, Classified

    Due to a software issue, there is the potential for a missing digit, letter, or decimal in either the "distance to target" or "tip stop point" display during navigation.

    Z-1776-2024 · Root cause: Software design · Recall details · FDA record ↗

Other Neurological stereotaxic Instrument devices

All Neurological stereotaxic Instrument devices →

Sources and updates

How reports and recalls are matched · Editorial policy · Report an error on this page