DRKClass 3
Dc-Defibrillator, High Energy, (Including Paddles)
FDA adverse event reports and recall history for dc-defibrillator, high energy, (including paddles) (product code DRK), from the public MAUDE/AEMS corpus and the live FDA recall database.
- Total reports
- 167
- Deaths
- 49
- Injuries
- 22
- Malfunctions
- 81
Reports per year
7092
6393
1794
295
198
199
205
107
408
111
113
115
219
123
Source: FDA adverse event reports by year received, 1992–2023. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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