Baxter Healthcare - Aibonito
FDA adverse event reports naming Baxter Healthcare - Aibonito as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: BAXTER HEALTHCARE - AIBONITO.
- Total reports
- 7,264
- Deaths
- 11
- Injuries
- 235
- Malfunctions
- 7,006
Reports per year
2809
30310
85711
1,49712
88613
88314
1,44615
60716
37317
19018
19319
120
Source: FDA adverse event reports by year received, 2009–2020. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Top device categories
- Set, Administration, IntravascularFPA4,559
- Container, I.V.KPE2,202
- Stopcock, I.V. SetFMG221
- Set, Blood TransfusionBRZ118
- Pump, InfusionFRN63
- Filter, Infusion LineFPB56
- System, Irrigation, UrologicalLJH23
- Set, I.V. Fluid TransferLHI14
- Needle, Hypodermic, Single LumenFMI3
- System, Peritoneal, Automatic DeliveryFKX2
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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