Baxter Healthcare - Cartago
FDA adverse event reports naming Baxter Healthcare - Cartago as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: BAXTER HEALTHCARE - CARTAGO.
- Total reports
- 1,786
- Deaths
- 0
- Injuries
- 17
- Malfunctions
- 1,769
Reports per year
111
212
313
214
215
17216
62917
41418
55919
220
Source: FDA adverse event reports by year received, 2011–2020. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Top device categories
- Set, Administration, IntravascularFPA1,665
- Set, Blood TransfusionBRZ60
- System, Irrigation, UrologicalLJH43
- Stopcock, I.V. SetFMG9
- Pump, InfusionFRN3
- Set, Administration, For Peritoneal Dialysis, DisposableKDJ2
- System, Peritoneal, Automatic DeliveryFKX1
- Set, I.V. Fluid TransferLHI1
- Pump, Infusion, ElastomericMEB1
- System/Device, Pharmacy CompoundingNEP1
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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