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
- 6,732
- Deaths
- 4
- Injuries
- 72
- Malfunctions
- 6,656
Reports per year
299
300
1201
103
71620
1,95321
2,19922
1,84023
224
325
126
Source: FDA adverse event reports by year received, 1999–2026. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Top device categories
- Set, Administration, IntravascularFPA6,638
- Syringe, PistonFMF32
- Catheter, Intravascular, Therapeutic, Short-Term Less Than 30 DaysFOZ21
- Set, I.V. Fluid TransferLHI16
- Closed Antineoplastic And Hazardous Drug Reconstitution And Transfer SystemONB11
- Saline, Vascular Access FlushNGT6
- Needle, Hypodermic, Single LumenFMI2
- Stopcock, I.V. SetFMG1
- Tubes, Vials, Systems, Serum Separators, Blood CollectionJKA1
- Container, I.V.KPE1
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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