Baxter Hlthcare Corp
FDA adverse event reports naming Baxter Hlthcare Corp as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: BAXTER HLTHCARE CORP.
- Total reports
- 6,772
- Deaths
- 0
- Injuries
- 1
- Malfunctions
- 6,771
Reports per year
312
2313
6,32214
42315
119
Source: FDA adverse event reports by year received, 2012–2019. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Top device categories
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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