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
- 34,842
- Deaths
- 21
- Injuries
- 321
- Malfunctions
- 34,500
Reports per year
197
117
15518
7719
4,04820
7,14021
17,41522
5,91023
9524
Source: FDA adverse event reports by year received, 1997–2024. Reporting paused twice in 2026 during FDA reporting-system changes and has since resumed.
Top device categories
- Pump, InfusionFRN23,334
- 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.
Monitor ST Paul automatically
DeviceWatch watches FDA adverse events and recalls for the products you care about, summarizes clinical narratives with AI and alerts you when a safety signal emerges.