Biohorizons, Inc.
FDA adverse event reports naming Biohorizons, Inc. as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: BIOHORIZONS, INC..
- Total reports
- 1,195
- Deaths
- 0
- Injuries
- 1,123
- Malfunctions
- 69
Reports per year
Source: FDA adverse event reports by year received, 2010–2026. 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 Biohorizons, Inc. automatically
DeviceWatch monitors available FDA adverse events and recalls. Growth includes event alerts for Death and Injury reports; Compliance Pro adds safety signals for investigation. FDA publication delays and incomplete collection or analysis coverage limit detection; no signal does not establish the absence of a safety concern. AI summaries and signals are provisional and require human review.