Hospira Ltd.
FDA adverse event reports naming Hospira Ltd. as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: HOSPIRA LTD..
- Total reports
- 1,740
- Deaths
- 1
- Injuries
- 41
- Malfunctions
- 1,692
Reports per year
5304
6105
7406
11007
35408
17909
11710
16011
18712
25613
14514
4215
216
Source: FDA adverse event reports by year received, 2004–2016. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Top device categories
- Set, Administration, IntravascularFPA1,336
- Tubing, Fluid DeliveryFPK200
- Bottle, Collection, VacuumKDQ72
- Pump, Infusion, PcaMEA28
- Apparatus, Suction, Operating-Room, Wall Vacuum PoweredGCX27
- Container, I.V.KPE26
- Filter, Infusion LineFPB23
- Pump, InfusionFRN10
- Catheter, IrrigationGBX9
- Port & Catheter, Implanted, Subcutaneous, IntravascularLJT3
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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