Sientra Inc
FDA adverse event reports naming Sientra Inc as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: SIENTRA INC.
- Total reports
- 3,582
- Deaths
- 0
- Injuries
- 3,564
- Malfunctions
- 17
Reports per year
319
120
121
1,13523
1,96924
47325
Source: FDA adverse event reports by year received, 2019–2025. 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 Sientra 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.