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 corpus and the live FDA recall database.
- Total reports
- 6,678
- Deaths
- 0
- Injuries
- 6,411
- Malfunctions
- 31
Reports per year
412
2113
4614
5215
30916
61417
62918
63519
69320
70921
71122
74223
62124
56925
28526
Source: FDA adverse event reports by year received, 2012–2026. 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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