MAHClass 2
Hearing Aid, Bone Conduction, Implanted
FDA adverse event reports and recall history for hearing aid, bone conduction, implanted (product code MAH), from the public MAUDE/AEMS corpus and the live FDA recall database.
- Total reports
- 6,650
- Deaths
- 0
- Injuries
- 6,383
- Malfunctions
- 31
Reports per year
412
2113
4614
5215
30916
61417
62918
63519
69220
70921
71122
74223
62124
56925
25826
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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