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
- 9,079
- Deaths
- 1,550
- Injuries
- 4,405
- Malfunctions
- 3,124
Reports per year
34525
8,73426
Source: FDA adverse event reports by year received, 2025–2026. Reporting paused during the 2026 MAUDE-to-AEMS transition 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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