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/AEMS 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 during the 2026 MAUDE-to-AEMS transition and has since resumed.
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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