ST. Jude Medical, Inc. - Cardiomems
FDA adverse event reports naming ST. Jude Medical, Inc. - Cardiomems as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: ST. JUDE MEDICAL, INC. - CARDIOMEMS.
- Total reports
- 2,202
- Deaths
- 51
- Injuries
- 901
- Malfunctions
- 1,250
Reports per year
2115
5816
28917
1,19718
36519
2420
3421
2022
3123
16324
Source: FDA adverse event reports by year received, 2015–2024. 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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