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
- 4,062
- Deaths
- 28
- Injuries
- 97
- Malfunctions
- 3,937
Reports per year
11817
12818
7819
23320
40121
53422
79623
68924
82925
25626
Source: FDA adverse event reports by year received, 2017–2026. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Top device categories
- Pump, InfusionFRN4,062
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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