Allergan (pringy)
FDA adverse event reports naming Allergan (pringy) as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: ALLERGAN (PRINGY).
- Total reports
- 8,708
- Deaths
- 4
- Injuries
- 7,387
- Malfunctions
- 1,317
Reports per year
214
32415
56816
1,34017
1,58118
91719
77320
83621
80222
93323
44524
17325
1426
Source: FDA adverse event reports by year received, 2014–2026. 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.
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