KRFClass 1
Charger, Pacemaker
FDA adverse event reports and recall history for charger, pacemaker (product code KRF), from the public MAUDE 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 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.
Monitor charger, pacemaker automatically
DeviceWatch watches FDA adverse events and recalls for the products you care about, summarizes clinical narratives with AI and alerts you when a safety signal emerges.