ST. Jude Medical Inc., Cardiac Rhythm Management D
FDA adverse event reports naming ST. Jude Medical Inc., Cardiac Rhythm Management D as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: ST. JUDE MEDICAL INC., CARDIAC RHYTHM MANAGEMENT D.
- Total reports
- 1,197
- Deaths
- 4
- Injuries
- 301
- Malfunctions
- 880
Top device categories
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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