Sistemas Medicos Alaris S.A DE C.V.
FDA adverse event reports naming Sistemas Medicos Alaris S.A DE C.V. as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: SISTEMAS MEDICOS ALARIS S.A DE C.V..
- Total reports
- 1,761
- Deaths
- 1
- Injuries
- 3
- Malfunctions
- 1,757
Reports per year
55925
1,20226
Source: FDA adverse event reports by year received, 2025–2026. 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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