HHDClass 1
Pad, Menstrual, Unscented
FDA adverse event reports and recall history for pad, menstrual, unscented (product code HHD), from the public MAUDE/AEMS corpus and the live FDA recall database.
- Total reports
- 136
- Deaths
- 0
- Injuries
- 82
- Malfunctions
- 27
Reports per year
512
313
414
615
416
417
518
619
220
521
822
1623
1524
1125
526
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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