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
- 1,267
- Deaths
- 74
- Injuries
- 803
- Malfunctions
- 390
Reports per year
423
19624
80325
26426
Source: FDA adverse event reports by year received, 2023–2026. 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.
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.