Baxter Healthcare - Mountain Home
FDA adverse event reports naming Baxter Healthcare - Mountain Home as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: BAXTER HEALTHCARE - MOUNTAIN HOME.
- Total reports
- 52,989
- Deaths
- 392
- Injuries
- 9,068
- Malfunctions
- 43,464
Reports per year
4908
33709
3,87210
8,28511
5,40112
8,59713
10,91014
8,62015
3,57116
1,08917
1,18018
1,07219
620
Source: FDA adverse event reports by year received, 2008–2020. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Top device categories
- System, Peritoneal, Automatic DeliveryFKX41,646
- Set, Administration, For Peritoneal Dialysis, DisposableKDJ11,201
- Container, Empty, For Collection & Processing Of Blood & Blood ComponentsKSR63
- Dialyzer, High Permeability With Or Without Sealed Dialysate SystemKDI54
- Pump, InfusionFRN14
- Clamp, LineFKK3
- System, Separation, Hematopoietic Stem CellMZK3
- Connector, Tubing, DialysateFKY2
- Set, Administration, IntravascularFPA2
- Product code ------1
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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