HHEClass 2
Cup, Menstrual
FDA adverse event reports and recall history for cup, menstrual (product code HHE), from the public MAUDE/AEMS corpus and the live FDA recall database.
- Total reports
- 550
- Deaths
- 0
- Injuries
- 372
- Malfunctions
- 167
Reports per year
110
212
214
215
116
417
118
2219
22020
4021
2622
13323
2924
3525
926
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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