Fresenius Vial S.a.s
FDA adverse event reports naming Fresenius Vial S.a.s as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: FRESENIUS VIAL S.A.S.
- Total reports
- 1,225
- Deaths
- 24
- Injuries
- 54
- Malfunctions
- 1,147
Reports per year
1016
15517
421
3222
35024
44425
23026
Source: FDA adverse event reports by year received, 2016–2026. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Top device categories
- Pump, InfusionFRN1,225
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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