Crutch
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 §890.3150 (Physical Medicine panel).
FDA MAUDE casebook
openFDA event book Crutch LIGHT-BOOK · MAUDE
#988 of 1000 · 373 reports · 1992–2026
- BOOK 373 reports
- RANK #988 of 1000
- DEATH 0 death-typed
- INJ 89 injury-typed
- MALF 81 malfunction
- SPAN 1992–2026
- PEAK 2013: 64
- PHOTO Probe, Thermodilution
Nearest event-volume peer: Probe, Thermodilution (0 report gap)
Crutch sits #988 of 1000 among tracked device types with 373 MAUDE reports spanning 1992–2026. 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
Crutch carries 21.7% MALFUNCTION-coded reports, 43.1pp below the 1,000-device-type mean, the widest gap of its three event codes. Codes are report labels, not adjudicated causation.
- DEATH 0.0% corpus 1.5% · below corpus mean (-1.5 pp)
- INJ 23.9% corpus 30.3% · below corpus mean (-6.4 pp)
- MALF 21.7% corpus 64.8% · below corpus mean (-43.1 pp)
Lead product-problem code Break is 37% of coded problems · Lead manufacturer UNKNOWN accounts for 79% of manufacturer-tagged reports · Top event location is 60% of location-tagged rows .
Crutch in the event-volume neighbourhood
FDA MAUDE report totals among this device type and nearest nationwide peers
- Crutch (this)
Crutch
373 reports
- Probe
Probe, Thermodilution
373 reports
- Azo Dye
Azo Dye, Calcium
372 reports
- Lens, Contact,
Lens, Contact, (Disposable)
372 reports
- Multi-Analyte…
Multi-Analyte Test System With Algorithmic Analysis For Detection Of Prostate Cancer
371 reports
- Antigens
Antigens, All Groups, Streptococcus Spp.
370 reports
What this shows Crutch carries 373 MAUDE reports, ranked #988 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 in 2025 (6) held close to the prior two-year average of 5.
Related Entities for Crutch
Top Manufacturers
Event Locations
Nationwide devices with a comparable report-volume footprint
Crutch carries zero death-typed MAUDE reports, so the peer set below compares report volume only; both axes are floored at ≥100 reports so the neighborhood stays in the advertised mass.
Similar report volume
Nearest other device types by FDA MAUDE report count (373 here).
Similar death-typed counts
Nearest other device types by death-typed report count (0 here), distinct from the volume row.
Read our methodology - how this data is sourced, computed, and verified.
Disclaimer: MAUDE figures for Crutch 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 Crutch; 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.