Baxter Healthcare (sg)
FDA adverse event reports naming Baxter Healthcare (sg) as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: BAXTER HEALTHCARE (SG).
- Total reports
- 10,237
- Deaths
- 32
- Injuries
- 119
- Malfunctions
- 10,036
Reports per year
24201
6,24902
1,07303
8904
55705
20406
10407
1,65608
2109
4010
115
116
Source: FDA adverse event reports by year received, 2001–2016. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Top device categories
- Pump, InfusionFRN9,782
- Pump, Infusion, PcaMEA385
- Set, Administration, IntravascularFPA38
- Catheter, Intravascular, Therapeutic, Short-Term Less Than 30 DaysFOZ16
- System, Peritoneal, Automatic DeliveryFKX9
- Bed, Ac-Powered Adjustable HospitalFNL2
- Transcervical Contraceptive Tubal Occlusion DeviceHHS2
- Product code ------1
- Product code 2692691
- Device, Counter-Pulsating, ExternalDRN1
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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