Defibtech, L.l.c.
FDA adverse event reports naming Defibtech, L.l.c. as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: DEFIBTECH, L.L.C..
- Total reports
- 5,065
- Deaths
- 20
- Injuries
- 6
- Malfunctions
- 5,038
Reports per year
315
1616
2317
1618
2219
1120
2021
1122
22923
1,34524
2,20725
1,16226
Source: FDA adverse event reports by year received, 2015–2026. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Top device categories
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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