Med-el Elektromedizinische Geraete Gmbh
FDA adverse event reports naming Med-el Elektromedizinische Geraete Gmbh as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: MED-EL ELEKTROMEDIZINISCHE GERAETE GMBH.
- Total reports
- 13,988
- Deaths
- 4
- Injuries
- 6,544
- Malfunctions
- 7,382
Reports per year
17712
20013
25314
74415
91516
1,11317
1,05118
1,02719
89020
1,16121
1,00622
1,17223
1,18224
1,25425
60126
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
- Implant, CochlearMCM12,861
- Implant, Hearing, Active, Middle Ear, Partially ImplantedMPV738
- Active Implantable Bone Conduction Hearing SystemPFO371
- Cochlear Implant With Combined Electrical Stimulation And Acoustic AmplificationPGQ6
- Barrier, Absorbable, AdhesionMCN5
- Prosthesis, Partial Ossicular ReplacementETB2
- Hearing Aid, Bone Conduction, ImplantedMAH2
- Ventilator, Continuous, Facility UseCBK1
- Replacement, Ossicular Prosthesis, TotalETA1
- Stimulator, Autonomic Nerve, Implanted For EpilepsyLYJ1
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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