Kestra Medical Technologies, Inc.
FDA adverse event reports naming Kestra Medical Technologies, Inc. as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: KESTRA MEDICAL TECHNOLOGIES, INC..
- Total reports
- 1,168
- Deaths
- 46
- Injuries
- 7
- Malfunctions
- 1,115
Reports per year
3822
27423
21524
38925
25226
Source: FDA adverse event reports by year received, 2022–2026. 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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