Back to Cranial / Stereotactic
Medtronic Pedicle Probe
No active recall
Manufacturer: Medtronic · FDA product code: HAW · Category: Neurological Stereotaxic Instrument
Severity Snapshot
121 total reports2011-01 – 2023-06 date range5.1% physician / facility reported94.9% manufacturer reported8 SKU variants
Failure & Consequence Profiles
Top Failure Modes
Click any bar to view those reports ↓
Top Patient Outcomes
Click any bar to view those reports ↓
Reporting Trend
Annual Reporting Volume
Click any bar to view those reports ↓
Note: the 2018 Voluntary Malfunction Summary Reporting expansion means volume increases may reflect surveillance changes, not increased device risk.
Reported Events
Submitted to FDA MAUDE by physicians, hospitals, manufacturers, and patients.
Filter by failure mode
Filter by outcome
Loading reports…