HHEClass 2
Cup, Menstrual
FDA adverse event reports and recall history for cup, menstrual (product code HHE), from the public MAUDE corpus and the live FDA recall database.
- Total reports
- 553
- Deaths
- 0
- Injuries
- 373
- Malfunctions
- 169
Reports per year
110
212
214
215
116
417
118
2219
22020
4021
2622
13323
2924
3525
1226
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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