Baxter International Inc.
FDA adverse event reports naming Baxter International Inc. as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: BAXTER INTERNATIONAL INC..
- Total reports
- 4,906
- Deaths
- 9
- Injuries
- 87
- Malfunctions
- 4,806
Reports per year
101
106
114
516
2317
3018
1119
2420
7021
16422
43723
3,86824
25125
2026
Source: FDA adverse event reports by year received, 2001–2026. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Top device categories
- Pump, InfusionFRN2,894
- Set, Administration, For Peritoneal Dialysis, DisposableKDJ891
- Set, Administration, IntravascularFPA659
- System, Peritoneal, Automatic DeliveryFKX317
- Container, I.V.KPE40
- Set, Blood TransfusionBRZ35
- Set, I.V. Fluid TransferLHI21
- Stopcock, I.V. SetFMG13
- Dialyzer, High Permeability With Or Without Sealed Dialysate SystemKDI8
- Infusion Safety Management SoftwarePHC8
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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