Allergan (costa Rica)
FDA adverse event reports naming Allergan (costa Rica) as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: ALLERGAN (COSTA RICA).
- Total reports
- 179,944
- Deaths
- 66
- Injuries
- 178,784
- Malfunctions
- 1,094
Reports per year
411
513
514
23815
14516
4,79717
8,71918
19,00419
22,03120
18,33821
26,41422
21,91223
22,11424
22,44925
13,76926
Source: FDA adverse event reports by year received, 2011–2026. Reporting paused twice in 2026 during FDA reporting-system changes and has since resumed.
Top device categories
- Prosthesis, Breast, Noninflatable, Internal, Silicone Gel-FilledFTR118,186
- Prosthesis, Breast, Inflatable, Internal, SalineFWM59,621
- Tissue Expander And AccessoriesLCJ1,763
- Implant, Intragastric For Morbid ObesityLTI182
- Mammary SizerMRD175
- Product code --13
- Kit, Surgical Instrument, DisposableKDD2
- Cover, Mattress (Medical Purposes)FMW1
- Implant, Dermal, For Aesthetic UseLMH1
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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