Hospira Costa Rica Ltd.
FDA adverse event reports naming Hospira Costa Rica Ltd. as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: HOSPIRA COSTA RICA LTD..
- Total reports
- 15,673
- Deaths
- 51
- Injuries
- 248
- Malfunctions
- 15,326
Reports per year
106
27109
26610
83811
1,26012
5,67213
6,13214
95615
6316
15117
6318
Source: FDA adverse event reports by year received, 2006–2018. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Top device categories
- Pump, InfusionFRN13,933
- Set, Administration, IntravascularFPA930
- Pump, Infusion, PcaMEA692
- Tubing, Fluid DeliveryFPK65
- Instrument, Surgical, DisposableKDC21
- Transducer, Blood-Pressure, ExtravascularDRS10
- Filter, Infusion LineFPB5
- Set, Blood TransfusionBRZ4
- Microfilter, Blood TransfusionCAK4
- Container, I.V.KPE4
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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