Baxter Healthcare - Cleveland
FDA adverse event reports naming Baxter Healthcare - Cleveland as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: BAXTER HEALTHCARE - CLEVELAND.
- Total reports
- 9,702
- Deaths
- 153
- Injuries
- 3,823
- Malfunctions
- 5,715
Reports per year
108
709
36510
1,63511
1,04512
1,38613
1,61314
2,91815
38516
21817
6318
6519
120
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
- Dialyzer, High Permeability With Or Without Sealed Dialysate SystemKDI8,088
- Set, Administration, For Peritoneal Dialysis, DisposableKDJ561
- Set, I.V. Fluid TransferLHI509
- Set, Administration, IntravascularFPA213
- Apparatus, Suction, Single Patient Use, Portable, NonpoweredGCY97
- Stopcock, I.V. SetFMG81
- Container, I.V.KPE78
- System, Peritoneal, Automatic DeliveryFKX27
- Filter, Infusion LineFPB22
- Equipment, Laboratory, General Purpose, Labeled Or Promoted For A Specific Medical UseLXG8
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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