Baxter Healthcare - Singapore
FDA adverse event reports naming Baxter Healthcare - Singapore as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: BAXTER HEALTHCARE - SINGAPORE.
- Total reports
- 73,286
- Deaths
- 485
- Injuries
- 581
- Malfunctions
- 72,135
Reports per year
508
45709
3,79710
37,29511
11,41012
4,65513
6,28414
5,93815
1,77216
1,01017
44918
21419
Source: FDA adverse event reports by year received, 2008–2019. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Top device categories
- Pump, InfusionFRN56,977
- System, Peritoneal, Automatic DeliveryFKX14,170
- Set, Administration, IntravascularFPA1,918
- Set, Blood TransfusionBRZ111
- Product code ------48
- Set, Administration, For Peritoneal Dialysis, DisposableKDJ32
- Pump, Infusion, PcaMEA21
- Pump, Infusion, ElastomericMEB3
- Stopcock, I.V. SetFMG2
- Clamp, LineFKK1
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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