2026 data FDA MAUDE openFDA

Scissors, General, Surgical

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 Scissors, General, Surgical LIGHT-BOOK · MAUDE

#726 of 1000 · 786 reports · 1992–2026

  • BOOK 786 reports
  • RANK #726 of 1000
  • DEATH 1 death-typed
  • INJ 149 injury-typed
  • MALF 568 malfunction
  • SPAN 1992–2026
  • PEAK 1997: 56
  • PHOTO Device

Nearest event-volume peer: Device, Fixation, Tracheal Tube (1 report gap)

Scissors, General, Surgical sits #726 of 1000 among tracked device types with 786 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 →

Event-type mix vs corpus

Shares of FDA event_type codes on this device type, compared with the mean across 1,000 device types that have ≥100 MAUDE reports. Codes are report labels, not adjudicated causation.

  • DEATH 0.1% corpus 1.5% · below corpus mean (-1.4 pp)
  • INJ 19.0% corpus 30.4% · below corpus mean (-11.5 pp)
  • MALF 72.3% corpus 64.5% · above corpus mean (+7.8 pp)

Lead product-problem code Break is 48% of coded problems · Lead manufacturer AESCULAP AG accounts for 33% of manufacturer-tagged reports · Top event location is 45% of location-tagged rows .

Scissors, General, Surgical in the event-volume neighbourhood

FDA MAUDE report totals among this device type and nearest nationwide peers

reports

What this shows Scissors, General, Surgical carries 786 MAUDE reports, ranked #726 of 1000.

Source FDA MAUDE via openFDA, aggregated by PlainHospital As of August 2026

Event Types

Malfunction 568 (72.3%)
Injury 149 (19.0%)
Other 43 (5.5%)
25 (3.2%)
Death 1 (0.1%)

Patient Outcomes

FDA patient-outcome codes (separate from event_type). Percentages use this chart's row total.

483 (59.8%)
Other 149 (18.4%)
Required Intervention 129 (16.0%)
R 17 (2.1%)
Hospitalization 16 (2.0%)
Disability 7 (0.9%)
S 4 (0.5%)
L 1 (0.1%)
Death 1 (0.1%)
Invalid Data 1 (0.1%)

Top Product Problems

Break 110
Material Fragmentation 27
Fracture 21
Contamination /Decontamination Problem 8
Delivered as Unsterile Product 8
Material Integrity Problem 7
Detachment Of Device Component 6
Detachment of Device or Device Component 6
Mechanical Problem 6
Failure to Cut 5
Material Separation 4
Adverse Event Without Identified Device or Use Problem 3
Device Markings/Labelling Problem 3
Inaccurate Information 3
Product Quality Problem 3
Component Missing 2
Defective Device 2
Device Fell 2
Dull, Blunt 2
Failure to Align 2

Yearly Trend

92
1992: 1
93
1993: 6
94
1994: 19
95
1995: 11
96
1996: 23
97
1997: 56
98
1998: 41
99
1999: 12
00
2000: 13
01
2001: 15
02
2002: 6
03
2003: 17
04
2004: 28
05
2005: 33
06
2006: 25
07
2007: 48
08
2008: 33
09
2009: 37
10
2010: 41
11
2011: 28
12
2012: 16
13
2013: 28
14
2014: 23
15
2015: 15
16
2016: 27
17
2017: 18
18
2018: 25
19
2019: 39
20
2020: 21
21
2021: 17
22
2022: 16
23
2023: 7
24
2024: 18
25
2025: 19
26
2026: 4

Related Entities for Scissors, General, Surgical

Event Locations

354 (45.0%)
HOSPITAL 219 (27.9%)
I 120 (15.3%)
INVALID DATA 42 (5.3%)
AMBULATORY SURGICAL FACILITY 16 (2.0%)
NO INFORMATION 14 (1.8%)
OTHER 8 (1.0%)
OUTPATIENT TREATMENT FACILITY 5 (0.6%)
OUTPATIENT DIAGNOSTIC FACILITY 4 (0.5%)
UNKNOWN 3 (0.4%)
AMBULATORY SURGICAL CENTER 1 (0.1%)

Compare AESCULAP AG vs UNK →

Nationwide devices with similar MAUDE profiles

Two openFDA-derived peer sets for Scissors, General, Surgical, both floored at ≥100 reports so the neighborhoods stay in the advertised mass.

Similar report volume

Nearest other device types by FDA MAUDE report count (786 here).

Similar death-typed counts

Nearest other device types by death-typed report count (1 here), distinct from the volume row.

Disclaimer: MAUDE figures for Scissors, General, 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 Scissors, General, 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.