NHWClass 2
Electrode, Pacing And Cardioversion, Temporary, Epicardial
FDA adverse event reports and recall history for electrode, pacing and cardioversion, temporary, epicardial (product code NHW), from the public MAUDE/AEMS corpus and the live FDA recall database.
- Total reports
- 125
- Deaths
- 2
- Injuries
- 91
- Malfunctions
- 31
Reports per year
102
103
308
409
1410
5011
2312
2513
115
117
122
123
Source: FDA adverse event reports by year received, 2002–2023. 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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