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
- 15,671
- Deaths
- 51
- Injuries
- 243
- Malfunctions
- 15,329
Reports per year
106
27109
26610
84111
1,25612
5,67113
6,13214
95615
6316
15117
6318
Source: FDA adverse event reports by year received, 2006–2018. Reporting paused twice in 2026 during FDA reporting-system changes and has since resumed.
Top device categories
- Pump, InfusionFRN13,930
- Set, Administration, IntravascularFPA932
- Pump, Infusion, PcaMEA693
- Tubing, Fluid DeliveryFPK65
- Instrument, Surgical, DisposableKDC21
- Transducer, Blood-Pressure, ExtravascularDRS10
- Filter, Infusion LineFPB5
- Set, Blood TransfusionBRZ4
- Container, I.V.KPE4
- Tube, Aspirating, Flexible, ConnectingBYY3
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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