MDT POWERED SURGICAL SOLUTIONS

Manufacturer adverse-event records for MDT POWERED SURGICAL SOLUTIONS come from the U.S. Food & Drug Administration (FDA) MAUDE database via openFDA, refreshed March 2026 - see our methodology. Not medical advice.

FDA MAUDE device safety record · 2010–2026 · mid-book · quiet Death-code · injury-light

Death-code intensity

MDT POWERED SURGICAL SOLUTIONS is quieter on Death-coded events

Death-coded event_type rows are 1 of 10,864 (0.01% · quiet tercile among 434 manufacturers). Absolute volume is mid-book.

What the Death-code reading shows for MDT POWERED SURGICAL SOLUTIONS

The standout signal for MDT POWERED SURGICAL SOLUTIONS is Death-code intensity: 0.01% of 10,864 reports (quiet tercile), while absolute volume is mid-book.

Mid-pack volume still shows a clear device fingerprint; the table below is the actionable layer for MDT POWERED SURGICAL SOLUTIONS. Event_type Death/Injury codes differ from patient-outcome rows - see methodology.

Reports span 12 device types, led in this extract by Malfunction at 10,471 (96.4% of event_type total). Peak single-year volume reaches 5,508 reports across 17 years. These are raw FDA submissions, not adjudicated findings. Snapshot . Verify current communications on the FDA MDR page.

10,864
Total Reports
1
Event-type Death
392
Injury Reports
12
Device Types

Event Types

Malfunction 10,471 (96.4%)
Injury 392 (3.6%)
Death 1 (0.0%)

Patient Outcomes

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

9,212 (95.7%)
Other 351 (3.6%)
Required Intervention 41 (0.4%)
O 4 (0.0%)
Hospitalization 4 (0.0%)
H 3 (0.0%)
R 2 (0.0%)
L 1 (0.0%)
Death 1 (0.0%)
Disability 1 (0.0%)
Life Threatening 1 (0.0%)

Yearly Trend

10
2010: 44
11
2011: 142
12
2012: 117
13
2013: 70
14
2014: 60
15
2015: 64
16
2016: 49
17
2017: 31
18
2018: 59
19
2019: 107
20
2020: 120
21
2021: 295
22
2022: 277
23
2023: 314
24
2024: 1,236
25
2025: 2,371
26
2026: 5,508