ICU Medical DE Mexico, S. DE R.L. DE C.V.
FDA adverse event reports naming ICU Medical DE Mexico, S. DE R.L. DE C.V. as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: ICU MEDICAL DE MEXICO, S. DE R.L. DE C.V..
- Total reports
- 8,163
- Deaths
- 26
- Injuries
- 144
- Malfunctions
- 7,993
Reports per year
217
17618
43119
54520
28721
34222
1,21223
1,92424
2,32425
92026
Source: FDA adverse event reports by year received, 2017–2026. Reporting paused twice in 2026 during FDA reporting-system changes and has since resumed.
Top device categories
- Set, Administration, IntravascularFPA3,431
- Stopcock, I.V. SetFMG2,519
- Closed Antineoplastic And Hazardous Drug Reconstitution And Transfer SystemONB1,386
- Transducer, Blood-Pressure, ExtravascularDRS666
- Catheter, Continuous FlushKRA48
- Catheter, Intravascular, DiagnosticDQO37
- Syringe, PistonFMF17
- Set, I.V. Fluid TransferLHI12
- Pump, InfusionFRN10
- Tubes, Gastrointestinal (And Accessories)KNT7
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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