Single-Use Reprocessed Ultrasonic Surgical Instruments
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 MAUDE casebook
openFDA event book Single-Use Reprocessed Ultrasonic Surgical… LIGHT-BOOK · MAUDE
#670 of 1000 · 980 reports · 2007–2026
- BOOK 980 reports
- RANK #670 of 1000
- DEATH 3 death-typed
- INJ 143 injury-typed
- MALF 827 malfunction
- SPAN 2007–2026
- PEAK 2012: 113
- PHOTO Container, Sharps
Nearest event-volume peer: Container, Sharps (1 report gap)
Single-Use Reprocessed Ultrasonic Surgical Instruments sits #670 of 1000 among tracked device types with 980 MAUDE reports spanning 2007–2026. 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 → · Similar-volume device →
Malfunction reports run above the device-type norm
Single-Use Reprocessed Ultrasonic Surgical… carries 84.4% MALFUNCTION-coded reports, 19.6pp above the 1,000-device-type mean, the widest gap of its three event codes. Codes are report labels, not adjudicated causation.
- DEATH 0.3% corpus 1.5% · below corpus mean (-1.2 pp)
- INJ 14.6% corpus 30.3% · below corpus mean (-15.7 pp)
- MALF 84.4% corpus 64.8% · above corpus mean (+19.6 pp)
Lead product-problem code Break is 22% of coded problems · Top event location is 58% of location-tagged rows .
Single-Use Reprocessed Ultrasonic Surgical… in the event-volume neighbourhood
FDA MAUDE report totals among this device type and nearest nationwide peers
- Pack
Pack, Hot Or Cold, Water Circulating
984 reports
- Midline Cathe…
Midline Catheter
983 reports
- Hepatitis A T…
Hepatitis A Test (Antibody And Igm Antibody)
982 reports
- Single-Use Re… (this)
Single-Use Reprocessed Ultrasonic Surgical Instruments
980 reports
- Container
Container, Sharps
979 reports
- Bronchoscope…
Bronchoscope Accessory
977 reports
What this shows Single-Use Reprocessed Ultrasonic Surgical Instruments carries 980 MAUDE reports, ranked #670 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 rose to 44 in 2025, up from an average of 18 in the two years before - a recent-year increase, not a lifetime pattern.
Related Entities for Single-Use Reprocessed Ultrasonic Surgical Instruments
Event Locations
Nationwide devices with a comparable volume-and-death footprint
Two openFDA-derived peer sets for Single-Use Reprocessed Ultrasonic Surgical…: 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 (980 here).
Similar death-typed counts
Nearest other device types by death-typed report count (3 here), distinct from the volume row.
Read our methodology - how this data is sourced, computed, and verified.
Disclaimer: MAUDE figures for Single-Use Reprocessed Ultrasonic Surgical… 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 Single-Use Reprocessed Ultrasonic Surgical…; 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.