Abbott Vascular-vascular Solutions
FDA adverse event reports naming Abbott Vascular-vascular Solutions as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: ABBOTT VASCULAR-VASCULAR SOLUTIONS.
- Total reports
- 2,201
- Deaths
- 88
- Injuries
- 1,665
- Malfunctions
- 434
Reports per year
206
31207
35808
42209
1,10710
Source: FDA adverse event reports by year received, 2006–2010. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Top device categories
- Stent, CarotidNIM826
- Device, Hemostasis, VascularMGB655
- Stents, Drains And Dilators For The Biliary DuctsFGE294
- Temporary Carotid Catheter For Embolic CaptureNTE197
- Catheter, Angioplasty, Peripheral, TransluminalLIT183
- Temporary Coronary Saphenous Vein Bypass Graft For Embolic ProtectionNFA27
- Wire, Guide, CatheterDQX15
- Stent, CoronaryMAF2
- Catheter, PercutaneousDQY1
- Catheters, Transluminal Coronary Angioplasty, PercutaneousLOX1
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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