KRFClass 1
Charger, Pacemaker
FDA adverse event reports and recall history for charger, pacemaker (product code KRF), from the public MAUDE/AEMS corpus and the live FDA recall database.
- Total reports
- 626
- Deaths
- 22
- Injuries
- 1
- Malfunctions
- 602
Reports per year
397
2198
20899
39200
101
102
Source: FDA adverse event reports by year received, 1997–2002. 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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