Guidant Vascular Intervention
FDA adverse event reports naming Guidant Vascular Intervention as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: GUIDANT VASCULAR INTERVENTION.
- Total reports
- 4,011
- Deaths
- 173
- Injuries
- 2,552
- Malfunctions
- 1,268
Reports per year
196
297
14598
40399
31800
38401
47302
45903
47204
49005
66606
19807
Source: FDA adverse event reports by year received, 1996–2007. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Top device categories
- Stent, CoronaryMAF2,158
- Wire, Guide, CatheterDQX785
- Catheters, Transluminal Coronary Angioplasty, PercutaneousLOX608
- Stents, Drains And Dilators For The Biliary DuctsFGE151
- Stent, CarotidNIM62
- Catheter, Angioplasty, Peripheral, TransluminalLIT58
- Catheter, Coronary, AtherectomyMCX54
- Introducer, CatheterDYB40
- Temporary Coronary Saphenous Vein Bypass Graft For Embolic ProtectionNFA32
- Intravascular Radiation Delivery SystemMOU24
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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