Cane
Adverse-event figures are drawn from the U.S. Food & Drug Administration (FDA) MAUDE database, refreshed March 2026, see our methodology.
OpenFDA device adverse-event casebook.
FDA Class I (lowest regulatory risk tier, general controls), regulated under 21 CFR §890.3075 (Physical Medicine panel).
FDA MAUDE casebook
openFDA event book Cane LIGHT-BOOK · MAUDE
#904 of 1000 · 484 reports · 1993–2026
- BOOK 484 reports
- RANK #904 of 1000
- DEATH 5 death-typed
- INJ 137 injury-typed
- MALF 152 malfunction
- SPAN 1993–2026
- PEAK 2014: 96
- PHOTO Patient Examination G…
Nearest event-volume peer: Patient Examination Glove (0 report gap)
Cane sits #904 of 1000 among tracked device types with 484 MAUDE reports spanning 1993–2026. Rank counts report volume, not confirmed device fault. Event_type Death / Injury / Malfunction are one code per report — not the same population as patient-outcome rows ( methodology). Read with this device → · Lead manufacturer → · Similar-volume device →
Malfunction reports sit below the device-type norm
Cane carries 31.4% MALFUNCTION-coded reports, 33.4pp below the 1,000-device-type mean, the widest gap of its three event codes. Codes are report labels, not adjudicated causation.
- DEATH 1.0% corpus 1.5% · near corpus mean (-0.5 pp)
- INJ 28.3% corpus 30.3% · below corpus mean (-2.0 pp)
- MALF 31.4% corpus 64.8% · below corpus mean (-33.4 pp)
Lead product-problem code Break is 39% of coded problems · Lead manufacturer UNKNOWN accounts for 77% of manufacturer-tagged reports · Top event location is 65% of location-tagged rows .
Cane in the event-volume neighbourhood
FDA MAUDE report totals among this device type and nearest nationwide peers
- Joint
Joint, Knee, External Brace
489 reports
- Percutaneous…
Percutaneous Catheter For Creation Of An Arteriovenous Fistula For Hemodialysis Access
486 reports
- Cane (this)
Cane
484 reports
- Patient Exami…
Patient Examination Glove
484 reports
- Rongeur
Rongeur, Manual
482 reports
- Cardiac Cathe…
Cardiac Catheterization Kit
481 reports
What this shows Cane carries 484 MAUDE reports, ranked #904 of 1000.
Event Types
Patient Outcomes
FDA patient-outcome codes (separate from event_type). Percentages use this chart's row total.
Top Product Problems
Yearly Trend
Reports fell to 7 in 2025, down from an average of 12 in the two years before.
Related Entities for Cane
Top Manufacturers
Event Locations
Nationwide devices with a comparable volume-and-death footprint
Two openFDA-derived peer sets for Cane: nearest by total report volume and nearest by death-typed count, each floored at ≥100 reports so the neighborhoods stay in the advertised mass.
Similar report volume
Nearest other device types by FDA MAUDE report count (484 here).
Similar death-typed counts
Nearest other device types by death-typed report count (5 here), distinct from the volume row.
Read our methodology - how this data is sourced, computed, and verified.
Disclaimer: MAUDE figures for Cane are informational only and are not clinical advice. Report codes do not prove device causation. Consult a qualified clinician before acting on this data.
Every figure on PlainHospital is rendered directly from federal source data, no number is typed in by an editor. Event-type mix on this page is computed from FDA MAUDE codes for Cane; corpus means use device types with ≥100 reports. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error. Data current as of August 2026.