CAGClass 2
Circulator, Breathing-Circuit
FDA adverse event reports and recall history for circulator, breathing-circuit (product code CAG), from the public MAUDE/AEMS corpus and the live FDA recall database.
- Total reports
- 196
- Deaths
- 1
- Injuries
- 6
- Malfunctions
- 187
Reports per year
294
105
111
9514
4115
116
217
218
319
420
1321
922
1423
324
126
Source: FDA adverse event reports by year received, 1994–2026. 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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