Baxter Healthcare - Largo
FDA adverse event reports naming Baxter Healthcare - Largo as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: BAXTER HEALTHCARE - LARGO.
- Total reports
- 38,514
- Deaths
- 960
- Injuries
- 862
- Malfunctions
- 36,663
Reports per year
1408
13309
1,64510
2,95311
9,95712
8,14213
8,14414
7,08915
31916
8117
3018
719
Source: FDA adverse event reports by year received, 2008–2019. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Top device categories
- System, Peritoneal, Automatic DeliveryFKX38,030
- Set, Administration, For Peritoneal Dialysis, DisposableKDJ236
- System/Device, Pharmacy CompoundingNEP96
- Dialyzer, High Permeability With Or Without Sealed Dialysate SystemKDI93
- Pump, InfusionFRN17
- System, Dialysate Delivery, Single PatientFKP13
- Pump, Infusion, PcaMEA7
- System, Hemodialysis, Access Recirculation MonitoringMQS7
- System, Separation, Hematopoietic Stem CellMZK7
- Product code ------3
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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