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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
1,857
Deaths
1
Injuries
5
Malfunctions
1,851

Reports per year

25
26

Source: FDA adverse event reports by year received, 20252026. Reporting paused twice in 2026 during FDA reporting-system changes 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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