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
- 7,996
- Deaths
- 26
- Injuries
- 142
- Malfunctions
- 7,828
Reports per year
217
17618
43119
54520
28721
34222
1,21223
1,92424
2,32425
75326
Source: FDA adverse event reports by year received, 2017–2026. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Top device categories
- Set, Administration, IntravascularFPA3,337
- Stopcock, I.V. SetFMG2,478
- Closed Antineoplastic And Hazardous Drug Reconstitution And Transfer SystemONB1,362
- Transducer, Blood-Pressure, ExtravascularDRS661
- Catheter, Continuous FlushKRA48
- Catheter, Intravascular, DiagnosticDQO37
- Syringe, PistonFMF17
- Set, I.V. Fluid TransferLHI12
- Pump, InfusionFRN10
- Set, Tubing, Blood, With And Without Anti-Regurgitation ValveFJK6
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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