Costa Rica
FDA adverse event reports naming Costa Rica as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: COSTA RICA.
- Total reports
- 2,172
- Deaths
- 23
- Injuries
- 762
- Malfunctions
- 1,383
Reports per year
103
5404
18005
24506
28907
71108
45109
11714
715
316
721
9722
723
324
Source: FDA adverse event reports by year received, 2003–2024. Reporting paused twice in 2026 during FDA reporting-system changes and has since resumed.
Top device categories
- Implant, Intragastric For Morbid ObesityLTI1,903
- Catheter, Hemodialysis, ImplantedMSD95
- Prosthesis, Breast, Noninflatable, Internal, Silicone Gel-FilledFTR71
- Prosthesis, Breast, Inflatable, Internal, SalineFWM54
- Catheter, Peritoneal, Long-Term IndwellingFJS15
- Catheter, Angioplasty, Peripheral, TransluminalLIT13
- Catheter, Hemodialysis, Non-ImplantedMPB7
- Catheter, Umbilical ArteryFOS2
- Stocking, Medical Support (For General Medical Purposes)FQL2
- Catheter, Intravascular, Therapeutic, Long-Term Greater Than 30 DaysLJS2
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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