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 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 twice in 2026 during FDA reporting-system changes and has since resumed.
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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