ST Paul
FDA adverse event reports naming ST Paul as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: ST PAUL.
- Total reports
- 34,841
- Deaths
- 21
- Injuries
- 321
- Malfunctions
- 34,499
Reports per year
197
117
15518
7719
4,04820
7,13921
17,41522
5,91023
9524
Source: FDA adverse event reports by year received, 1997–2024. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Top device categories
- Pump, InfusionFRN23,333
- Set, Administration, IntravascularFPA7,777
- Pump, Infusion, PcaMEA1,168
- Warmer, Thermal, Infusion FluidLGZ865
- Warmer, Blood, Non-Electromagnetic RadiationBSB350
- Ventilator, Emergency, Powered (Resuscitator)BTL249
- Device, Warming. Blood And PlasmaKZL245
- Analyzer, Gas, Carbon-Dioxide, Gaseous-PhaseCCK188
- OximeterDQA119
- Port & Catheter, Implanted, Subcutaneous, IntravascularLJT108
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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