Allergan (irvine)
FDA adverse event reports naming Allergan (irvine) as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: ALLERGAN (IRVINE).
- Total reports
- 1,967
- Deaths
- 0
- Injuries
- 1,341
- Malfunctions
- 626
Reports per year
516
12717
17218
32719
30620
28121
18922
19623
15824
15325
5326
Source: FDA adverse event reports by year received, 2016–2026. 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.
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