Baxter Healthcare - Malta
FDA adverse event reports naming Baxter Healthcare - Malta as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: BAXTER HEALTHCARE - MALTA.
- Total reports
- 4,282
- Deaths
- 0
- Injuries
- 19
- Malfunctions
- 4,258
Reports per year
109
20910
82911
1,08112
63713
47314
55315
24316
11217
7518
6919
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, IntravascularFPA2,294
- Container, I.V.KPE822
- Set, I.V. Fluid TransferLHI660
- Set, Blood TransfusionBRZ322
- Stopcock, I.V. SetFMG94
- System, Irrigation, UrologicalLJH66
- Pump, InfusionFRN9
- Set, Administration, For Peritoneal Dialysis, DisposableKDJ5
- System, Peritoneal, Automatic DeliveryFKX2
- System/Device, Pharmacy CompoundingNEP2
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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