DTXClass 2
Gas Control Unit, Cardiopulmonary Bypass
FDA adverse event reports and recall history for gas control unit, cardiopulmonary bypass (product code DTX), from the public MAUDE/AEMS corpus and the live FDA recall database.
- Total reports
- 753
- Deaths
- 3
- Injuries
- 7
- Malfunctions
- 701
Reports per year
1112
913
2014
1615
3616
4117
4818
5319
6320
7721
6922
6923
7824
12725
3326
Source: FDA adverse event reports by year received, 2012–2026. 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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