Medtech Sa
FDA adverse event reports naming Medtech Sa as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: MEDTECH SA.
- Total reports
- 2,063
- Deaths
- 1
- Injuries
- 363
- Malfunctions
- 1,699
Reports per year
115
716
72217
36018
46219
33020
18121
Source: FDA adverse event reports by year received, 2015–2021. 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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