Abbott Vascular - Redwood City
FDA adverse event reports naming Abbott Vascular - Redwood City as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: ABBOTT VASCULAR - REDWOOD CITY.
- Total reports
- 2,754
- Deaths
- 12
- Injuries
- 2,654
- Malfunctions
- 83
Reports per year
307
37408
90709
1,47010
Source: FDA adverse event reports by year received, 2007–2010. Reporting paused twice in 2026 during FDA reporting-system changes and has since resumed.
Top device categories
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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