Christoph Miethke Gmbh & Co Kg
FDA adverse event reports naming Christoph Miethke Gmbh & Co Kg as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: CHRISTOPH MIETHKE GMBH & CO KG.
- Total reports
- 2,660
- Deaths
- 1
- Injuries
- 2,491
- Malfunctions
- 168
Reports per year
217
218
119
13420
55721
45622
43723
43224
44225
19726
Source: FDA adverse event reports by year received, 2017–2026. 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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