DWDClass 2
Suction Control, Intracardiac, Cardiopulmonary Bypass
FDA adverse event reports and recall history for suction control, intracardiac, cardiopulmonary bypass (product code DWD), from the public MAUDE corpus and the live FDA recall database.
- Total reports
- 108
- Deaths
- 0
- Injuries
- 30
- Malfunctions
- 75
Reports per year
110
111
112
1013
714
3815
616
1217
818
1319
220
122
123
124
126
Source: FDA adverse event reports by year received, 2010–2026. Reporting paused twice in 2026 during FDA reporting-system changes and has since resumed.
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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