THE Spectranetics Corporation
FDA adverse event reports naming THE Spectranetics Corporation as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: THE SPECTRANETICS CORPORATION.
- Total reports
- 1,341
- Deaths
- 190
- Injuries
- 829
- Malfunctions
- 322
Reports per year
106
107
117
15318
22919
26920
26421
28222
14123
Source: FDA adverse event reports by year received, 2006–2023. Reporting paused twice in 2026 during FDA reporting-system changes and has since resumed.
Top device categories
- Stylet, CatheterDRB423
- Device, Removal, Pacemaker Electrode, PercutaneousMFA376
- Dilator, Vessel, For Percutaneous CatheterizationDRE161
- Catheter, Peripheral, AtherectomyMCW135
- Device, Angioplasty, Laser, CoronaryLPC73
- Catheter, Intravascular Occluding, TemporaryMJN62
- Catheter, Percutaneous, Cutting/ScoringPNO41
- Drug-Eluting Peripheral Transluminal Angioplasty CatheterONU27
- Catheter, PercutaneousDQY22
- Catheter, Percutaneous Transluminal Coronary Angioplasty (Ptca), Cutting/ScoringNWX15
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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