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
- 9,756
- Deaths
- 1,657
- Injuries
- 4,612
- Malfunctions
- 3,487
Reports per year
34525
9,41126
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.
Monitor Abiomed, Inc. - 1220648 automatically
DeviceWatch watches FDA adverse events and recalls for the products you care about, summarizes clinical narratives with AI and alerts you when a safety signal emerges.