Baxter Healthcare - Cali
FDA adverse event reports naming Baxter Healthcare - Cali as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: BAXTER HEALTHCARE - CALI.
- Total reports
- 1,711
- Deaths
- 0
- Injuries
- 9
- Malfunctions
- 1,701
Reports per year
209
3710
27411
15512
23113
32214
22315
20216
15417
7018
4119
Source: FDA adverse event reports by year received, 2009–2019. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Top device categories
- Set, Administration, IntravascularFPA622
- Container, I.V.KPE344
- Dialyzer, High Permeability With Or Without Sealed Dialysate SystemKDI265
- Set, Administration, For Peritoneal Dialysis, DisposableKDJ263
- System, Peritoneal, Automatic DeliveryFKX77
- Set, Tubing, Blood, With And Without Anti-Regurgitation ValveFJK36
- Stopcock, I.V. SetFMG36
- System, Irrigation, UrologicalLJH23
- Dialysate Concentrate For Hemodialysis (Liquid Or Powder)KPO16
- Collector, Urine, (And Accessories) For Indwelling CatheterKNX13
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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