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
- 3,543
- Deaths
- 3
- Injuries
- 990
- Malfunctions
- 2,423
Reports per year
24005
26506
31907
31808
25809
23610
18311
29612
34213
56714
27815
116
424
125
226
Source: FDA adverse event reports by year received, 2005–2026. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Top device categories
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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