Baylis Medicale CIE Inc
FDA adverse event reports naming Baylis Medicale CIE Inc as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: BAYLIS MEDICALE CIE INC.
- Total reports
- 1,290
- Deaths
- 74
- Injuries
- 821
- Malfunctions
- 395
Reports per year
423
19524
80325
28826
Source: FDA adverse event reports by year received, 2023–2026. Reporting paused twice in 2026 during FDA reporting-system changes and has since resumed.
Top device categories
Recent recalls
No recalls listed in the FDA device recall database for this entry.
Monitor Baylis Medicale CIE Inc automatically
DeviceWatch watches FDA adverse events and recalls for the products you care about, summarizes clinical narratives with AI and alerts you when a safety signal emerges.