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
- 2,586
- Deaths
- 297
- Injuries
- 1,235
- Malfunctions
- 1,054
Top device categories
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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DeviceWatch monitors available FDA adverse events and recalls. Growth includes event alerts for Death and Injury reports; Compliance Pro adds safety signals for investigation. FDA publication delays and incomplete collection or analysis coverage limit detection; no signal does not establish the absence of a safety concern. AI summaries and signals are provisional and require human review.