OOBClass 3
Drug-Eluting Percutaneous Transluminal Coronary Angioplasty Catheter
FDA adverse event reports and recall history for drug-eluting percutaneous transluminal coronary angioplasty catheter (product code OOB), from the public MAUDE corpus and the live FDA recall database.
- Total reports
- 629
- Deaths
- 71
- Injuries
- 193
- Malfunctions
- 364
Reports per year
14124
23025
25826
Source: FDA adverse event reports by year received, 2024–2026. Reporting paused twice in 2026 during FDA reporting-system changes and has since resumed.
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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