Inhibitor, Peridural Fibrosis (Adhesion Barrier)
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 Inhibitor, Peridural Fibrosis LIGHT-BOOK · MAUDE
#935 of 1000 · 440 reports · 1999–2008
- BOOK 440 reports
- RANK #935 of 1000
- DEATH 2 death-typed
- INJ 420 injury-typed
- MALF 5 malfunction
- SPAN 1999–2008
- PEAK 2001: 324
- PHOTO Resectoscope
Nearest event-volume peer: Resectoscope, Working Element (0 report gap)
Inhibitor, Peridural Fibrosis (Adhesion Barrier) sits #935 of 1000 among tracked device types with 440 MAUDE reports spanning 1999–2008. 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 →
Injury-coded reports run above the device-type norm
Inhibitor, Peridural Fibrosis carries 95.5% INJURY-coded reports, 65.2pp above the 1,000-device-type mean, the widest gap of its three event codes. Codes are report labels, not adjudicated causation.
- DEATH 0.5% corpus 1.5% · below corpus mean (-1.1 pp)
- INJ 95.5% corpus 30.3% · above corpus mean (+65.2 pp)
- MALF 1.1% corpus 64.8% · below corpus mean (-63.7 pp)
Lead product-problem code Device remains implanted is 45% of coded problems · Top event location is 89% of location-tagged rows .
Inhibitor, Peridural Fibrosis in the event-volume neighbourhood
FDA MAUDE report totals among this device type and nearest nationwide peers
- System
System, X-Ray, Mammographic
443 reports
- Biliary Cathe…
Biliary Catheter For Stone Removal That May Also Allow For Irrigation And Contrast Injection
441 reports
- Inhibitor (this)
Inhibitor, Peridural Fibrosis (Adhesion Barrier)
440 reports
- Resectoscope
Resectoscope, Working Element
440 reports
- Lithotriptor
Lithotriptor, Electro-Hydraulic
438 reports
- Stimulator
Stimulator, Neuromuscular, Lower Back Muscles, Totally Implanted For Pain Relief
438 reports
What this shows Inhibitor, Peridural Fibrosis (Adhesion Barrier) carries 440 MAUDE reports, ranked #935 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 6 in 2003, down from an average of 173 in the two years before.
Related Entities for Inhibitor, Peridural Fibrosis (Adhesion Barrier)
Event Locations
Nationwide devices with a comparable volume-and-death footprint
Two openFDA-derived peer sets for Inhibitor, Peridural Fibrosis: 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 (440 here).
Similar death-typed counts
Nearest other device types by death-typed report count (2 here), distinct from the volume row.
Read our methodology - how this data is sourced, computed, and verified.
Disclaimer: MAUDE figures for Inhibitor, Peridural Fibrosis 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 Inhibitor, Peridural Fibrosis; 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.