Snare, Flexible
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 II (moderate risk, special controls required), regulated under 21 CFR §876.4300 (Gastroenterology, Urology panel).
FDA MAUDE casebook
openFDA event book Snare, Flexible LIGHT-BOOK · MAUDE
#335 of 1000 · 4,640 reports · 1994–2026
- BOOK 4,640 reports
- RANK #335 of 1000
- DEATH 10 death-typed
- INJ 593 injury-typed
- MALF 4,006 malfunction
- SPAN 1994–2026
- PEAK 2020: 487
- PHOTO Broach
Nearest event-volume peer: Broach (18 report gap)
Snare, Flexible sits #335 of 1000 among tracked device types with 4,640 MAUDE reports spanning 1994–2026. 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 run above the device-type norm
Snare, Flexible carries 86.3% MALFUNCTION-coded reports, 21.5pp above the 1,000-device-type mean, the widest gap of its three event codes. Codes are report labels, not adjudicated causation.
- DEATH 0.2% corpus 1.5% · below corpus mean (-1.3 pp)
- INJ 12.8% corpus 30.3% · below corpus mean (-17.5 pp)
- MALF 86.3% corpus 64.8% · above corpus mean (+21.5 pp)
Lead product-problem code Failure to Cut is 23% of coded problems · Lead manufacturer BOSTON SCIENTIFIC CORPORATION accounts for 54% of manufacturer-tagged reports · Top event location is 64% of location-tagged rows .
Snare, Flexible in the event-volume neighbourhood
FDA MAUDE report totals among this device type and nearest nationwide peers
- Closed Antine…
Closed Antineoplastic And Hazardous Drug Reconstitution And Transfer System
4,732 reports
- System
System, Nuclear Magnetic Resonance Imaging
4,713 reports
- Apparatus
Apparatus, Suction, Single Patient Use, Portable, Nonpowered
4,706 reports
- Table
Table, Obstetrical, Ac-Powered (And Accessories)
4,666 reports
- Snare (this)
Snare, Flexible
4,640 reports
- Broach
Broach
4,622 reports
What this shows Snare, Flexible carries 4,640 MAUDE reports, ranked #335 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 (277) held close to the prior two-year average of 244.
Related Entities for Snare, Flexible
Top Manufacturers
Event Locations
Compare BOSTON SCIENTIFIC CORPORATION vs BOSTON SCIENTIFIC - COSTA RICA (COYOL) →
Nationwide devices with a comparable volume-and-death footprint
Two openFDA-derived peer sets for Snare, Flexible: 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 (4,640 here).
Similar death-typed counts
Nearest other device types by death-typed report count (10 here), distinct from the volume row.
Read our methodology - how this data is sourced, computed, and verified.
Disclaimer: MAUDE figures for Snare, Flexible 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 Snare, Flexible; 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.