Abiomed, Inc. - 1220648
FDA adverse event reports naming Abiomed, Inc. - 1220648 as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: ABIOMED, INC. - 1220648.
- Total reports
- 9,718
- Deaths
- 1,656
- Injuries
- 4,595
- Malfunctions
- 3,467
Reports per year
34525
9,37326
Source: FDA adverse event reports by year received, 2025–2026. 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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