Allergan (pleasanton)
FDA adverse event reports naming Allergan (pleasanton) as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: ALLERGAN (PLEASANTON).
- Total reports
- 3,785
- Deaths
- 0
- Injuries
- 3,785
- Malfunctions
- 0
Reports per year
116
118
1919
1220
15321
3,59923
Source: FDA adverse event reports by year received, 2016–2023. 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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