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
- 6,929
- Deaths
- 12
- Injuries
- 33
- Malfunctions
- 6,883
Reports per year
1000
4201
1002
204
117
73423
1,90924
3,59525
62626
Source: FDA adverse event reports by year received, 2000–2026. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Top device categories
- Set, Administration, IntravascularFPA6,875
- Set, I.V. Fluid TransferLHI24
- Syringe, PistonFMF16
- Closed Antineoplastic And Hazardous Drug Reconstitution And Transfer SystemONB7
- Saline, Vascular Access FlushNGT2
- Needle, Hypodermic, Single LumenFMI1
- Pump, InfusionFRN1
- Instrument, Surgical, DisposableKDC1
- Device, Intravascular Catheter SecurementKMK1
- Container, SharpsMMK1
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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