Boston Scientific - Costa Rica (heredia)
FDA adverse event reports naming Boston Scientific - Costa Rica (heredia) as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: BOSTON SCIENTIFIC - COSTA RICA (HEREDIA).
- Total reports
- 1,943
- Deaths
- 45
- Injuries
- 694
- Malfunctions
- 1,203
Reports per year
311
5212
9313
26314
32415
38216
45317
37318
Source: FDA adverse event reports by year received, 2011–2018. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Top device categories
- Wire, Guide, CatheterDQX791
- Catheter, Coronary, AtherectomyMCX591
- Catheter, Percutaneous, Cardiac Ablation, For Treatment Of Atrial FlutterOAD294
- Catheter, Electrode Recording, Or Probe, Electrode RecordingDRF153
- Cardiac Ablation Percutaneous CatheterLPB36
- Stylet For Catheter, Gastro-UrologyEZB27
- Catheter, Peripheral, AtherectomyMCW25
- Catheter, Percutaneous, Cardiac Ablation, For Treatment Of Atrial FibrillationOAE17
- Bronchoscope (Flexible Or Rigid)EOQ6
- Cable, Transducer And Electrode, Patient, (Including Connector)DSA1
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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