Baxter Healthcare PTE. Ltd.
FDA adverse event reports naming Baxter Healthcare PTE. Ltd. as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: BAXTER HEALTHCARE PTE. LTD..
- Total reports
- 22,737
- Deaths
- 85
- Injuries
- 312
- Malfunctions
- 22,276
Reports per year
29997
50298
40899
27400
5701
10602
5,48203
1,32604
6,37505
2,98306
10207
3,99308
43309
35910
215
Source: FDA adverse event reports by year received, 1997–2015. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Top device categories
- Pump, InfusionFRN21,070
- Pump, Infusion, PcaMEA1,198
- System, Peritoneal, Automatic DeliveryFKX314
- Catheter, Intravascular, Therapeutic, Short-Term Less Than 30 DaysFOZ91
- Set, Administration, IntravascularFPA55
- Pump, Infusion, ElastomericMEB3
- Product code ------1
- Product code 2692691
- Hexokinase, GlucoseCFR1
- Product code FNRFNR1
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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