Devices › Neurological stereotaxic instrument
Device brand name · Neurological stereotaxic instrument
Medtronic Navigation: medical device reports filed with FDA
682 reports name it, 2018–2026. Manufacturer given most often on reports: Medtronic Navigation. Product code HAW.
- 682
- device reports naming the brand
- 0% of all MAUDE reports · about 88 a year
- 69
- reports, 12 months to August 2026
- 92 in the 12 months before
- 30.4%
- classified as malfunction
- 92.2% across the product code
- 6.7%
- classified as death, as reported
- 46 reports · not verified by FDA
FDA's MAUDE database holds 682 reports that name the brand "Medtronic Navigation" (neurological stereotaxic instrument), received between October 2018 and August 2026; the manufacturer given most often on reports is Medtronic Navigation. Spellings of one product vary from report to report.
69 reports arrived in the 12 months to August 2026, down 25% from 92 in the 12 months before. FDA releases MAUDE data monthly; reports can arrive months after an event, so the newest months grow in later releases. The event types recorded are injury (62.9%), malfunction (30.4%) and death (6.7%); across all neurological stereotaxic instrument reports (product code HAW) death is recorded in 0.2% and malfunction in 92.2%. Event type is the reporter's classification of the report, not a verified outcome.
The device problems coded most often are imprecision (13.9%), incorrect, inadequate or imprecise result or readings (10.7%) and material integrity problem (2.8%). The patient problems coded most often are hemorrhage/blood loss/bleeding, intracranial hemorrhage and cerebrospinal fluid leakage. FDA states that "MDR data alone cannot be used to establish rates of events, evaluate a change in event rates over time or compare event rates between devices. The number of reports cannot be interpreted or used in isolation to reach conclusions about the existence, severity, or frequency of problems associated with devices." It adds that the reporting system "has limitations, including the potential submission of incomplete, inaccurate, untimely, unverified, or biased data."
Reports by month, five years
Reports by the month FDA received them. FDA releases MAUDE data monthly; reports can arrive months after an event, so the newest months grow in later releases.
By year received
Event type and report source
Event type, as classified on the report
Who filed the report
Grey bar: all 42,840 reports carrying product code HAW. Event type is the filer's classification and is not verified by FDA.
Device problems coded
| Device problem (FDA code) | Reports | Share | Share across product code |
|---|---|---|---|
| Imprecision | 95 | 13.9% | 13% |
| Incorrect, inadequate or imprecise result or readings | 73 | 10.7% | 4.1% |
| Material integrity problema problem with the device material | 19 | 2.8% | 5.3% |
| Human-device interface problem | 16 | 2.3% | 7% |
| Mechanical problema mechanical problem | 13 | 1.9% | 10.9% |
| Device sensing problem | 12 | 1.8% | 6.1% |
| Application program freezes or fails to launch | 9 | 1.3% | 7.4% |
| Communication or transmission problemthe device could not communicate or transmit | 8 | 1.2% | 6.4% |
| Material fragmentation | 7 | 1% | 0.3% |
| Output problem | 4 | 0.6% | 1.8% |
| Activation, positioning or separation problem | 3 | 0.4% | 0.2% |
| Connection problema connection problem | 3 | 0.4% | 1.8% |
| Environmental compatibility problem | 3 | 0.4% | 3.1% |
| Excessive heating | 2 | 0.3% | 0.2% |
| Infusion or flow problema problem with flow or infusion | 2 | 0.3% | 0% |
| No device output | 2 | 0.3% | 0.2% |
| Application program problem | 1 | 0.1% | 6.3% |
| Biocompatibility | 1 | 0.1% | 0% |
| Contamination | 1 | 0.1% | 0% |
| Contamination /decontamination problem | 1 | 0.1% | 0% |
FDA's device problem codes as entered on the report; one report can carry several. Generic codes such as "no apparent adverse event" are left out.
Patient problems coded
| Patient problem (FDA code) | Reports | Share |
|---|---|---|
| Hemorrhage/blood loss/bleeding | 83 | 12.2% |
| Intracranial hemorrhage | 46 | 6.7% |
| Cerebrospinal fluid leakage | 43 | 6.3% |
| Muscle weakness/atrophy | 42 | 6.2% |
| Hematomaa collection of blood under the skin or in tissue | 39 | 5.7% |
| Dysphasia | 35 | 5.1% |
| Convulsion/seizure | 33 | 4.8% |
| Painpain, site not specified | 30 | 4.4% |
| Swelling/ edema | 30 | 4.4% |
| Post operative wound infection | 29 | 4.3% |
| Paresis | 28 | 4.1% |
| Visual impairmentreduced vision | 28 | 4.1% |
| Cognitive changes | 26 | 3.8% |
| No patient involvement | 23 | 3.4% |
| Hydrocephalus | 22 | 3.2% |
Patient problem codes are present mainly in reports filed since 2019 and are often blank.
In context
| Measure | Medtronic Navigation | Product code HAW | All MAUDE reports |
|---|---|---|---|
| Reports | 682 | 42,840 | 26,136,888 |
| Share of that pool | — | 1.6% | 0% |
| Classified as death, per 1,000 reports | 67 | 2 | 9 |
| Classified as injury | 62.9% | 6.9% | 36.2% |
| Classified as malfunction | 30.4% | 92.2% | 62.3% |
| Filed by the manufacturer | 100% | 99.5% | 94.9% |
Shares are of reports, not of devices in use. FDA states that "MDR data alone cannot be used to establish rates of events, evaluate a change in event rates over time or compare event rates between devices. The number of reports cannot be interpreted or used in isolation to reach conclusions about the existence, severity, or frequency of problems associated with devices." It adds that the reporting system "has limitations, including the potential submission of incomplete, inaccurate, untimely, unverified, or biased data."
Other brands with product code HAW
| Brand | Reports | Latest 12 months | Classified as death |
|---|---|---|---|
| StealthStation S8 system | 10,870 | 1,368 | 0.1% |
| Stealthstation S7 System | 5,989 | 0 | 0.4% |
| Stealthstation S7 | 2,207 | 30 | 0.4% |
| Fusion Navigation System | 2,165 | 0 | 0% |
| Fusion Ent Navigation System | 1,520 | 8 | 0% |
| Stealthstation S8 Premium System | 1,007 | 0 | 0% |
| Stealthstation Treon Treatment Guidance System | 961 | 0 | 0.4% |
| Cart 9734056 S7 Staff Shrt 100-120v Intl | 904 | 4 | 0% |
| Rosa Surgical Device | 711 | 0 | 0% |
| Rosa Brain | 675 | 0 | 0.1% |
| Rosa One | 595 | 0 | 0% |
| Stealthstation I7 Integrated Navigation System | 471 | 0 | 0% |
| Open Spine Clamp Titanium | 445 | 0 | 0% |
| Stealthstation S7 Navigation | 366 | 1 | 0% |
| S7 | 363 | 0 | 0% |
Ordered by report count for navigation only. FDA states that "MDR data alone cannot be used to establish rates of events, evaluate a change in event rates over time or compare event rates between devices. The number of reports cannot be interpreted or used in isolation to reach conclusions about the existence, severity, or frequency of problems associated with devices." It adds that the reporting system "has limitations, including the potential submission of incomplete, inaccurate, untimely, unverified, or biased data." FDA also states that "common products may have a higher number of adverse events due to the higher total number of people using the product."
Questions about Medtronic Navigation reports
How many FDA reports name Medtronic Navigation?
682 medical device reports in the openFDA MAUDE release of 28 Sep 2026, covering reports received through August 2026; 69 in the latest 12 months.
What kinds of events are reported?
injury (62.9%), malfunction (30.4%) and death (6.7%). "Event type" is how the report was classified when filed: death, injury, malfunction or other.
What device problems are coded?
imprecision (13.9%), incorrect, inadequate or imprecise result or readings (10.7%), material integrity problem (2.8%), human-device interface problem (2.3%) and mechanical problem (1.9%). These are FDA's device problem codes as entered on the report.
Who files these reports?
manufacturer reports (100%). Manufacturers and user facilities are required to report; voluntary reports come from health professionals and the public.
Do these reports show that Medtronic Navigation was at fault?
No. FDA states that "MDR data alone cannot be used to establish rates of events, evaluate a change in event rates over time or compare event rates between devices. The number of reports cannot be interpreted or used in isolation to reach conclusions about the existence, severity, or frequency of problems associated with devices." It adds that the reporting system "has limitations, including the potential submission of incomplete, inaccurate, untimely, unverified, or biased data." FDA adds that "a causal relationship cannot be established between product and reactions listed in a report."
How do I report a problem with a medical device?
Through FDA MedWatch (Form FDA 3500 for health professionals and consumers), or to the manufacturer. See the guide on how to report.
Where this comes from. Counts are built from the openFDA Device Adverse Event (MAUDE) bulk export released 28 Sep 2026, which holds reports FDA received through 31 Aug 2026. Brand, generic and manufacturer names are as written on the reports; product code names come from FDA's device classification. A report counts here when any device it lists carries this brand name after punctuation and capitalisation are normalised. No report narrative, lot number, patient detail or reporter identity is published. See the methodology and sources; FDA's record is authoritative, and corrections are handled within five working days.
Drug data (FAERS) through 30 Jun 2026; device data (MAUDE) through 31 Aug 2026. Not medical advice.