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
- 2,097
- Deaths
- 0
- Injuries
- 2,089
- Malfunctions
- 7
Reports per year
208
209
210
313
414
115
116
718
63019
75120
65221
1922
1323
1024
Source: FDA adverse event reports by year received, 2008–2024. 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.
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