Cochlear Bone Anchored Solutions Ab
FDA adverse event reports naming Cochlear Bone Anchored Solutions Ab as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: COCHLEAR BONE ANCHORED SOLUTIONS AB.
- Total reports
- 12,634
- Deaths
- 2
- Injuries
- 12,584
- Malfunctions
- 34
Reports per year
31312
61413
54014
81415
88916
84117
86918
1,06719
1,22020
1,17421
1,08322
1,12623
81024
79325
39626
Source: FDA adverse event reports by year received, 2012–2026. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Top device categories
- Hearing Aid, Bone ConductionLXB6,650
- Hearing Aid, Bone Conduction, ImplantedMAH5,656
- Prosthesis, Nose, InternalFZE195
- Implant, CochlearMCM70
- Active Implantable Bone Conduction Hearing SystemPFO58
- Pelvimeter, InternalLBX3
- Motor, Surgical Instrument, Ac-PoweredGEY1
- Cochlear Implant With Combined Electrical Stimulation And Acoustic AmplificationPGQ1
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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