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
- 1,449
- Deaths
- 180
- Injuries
- 702
- Malfunctions
- 567
Top device categories
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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