Altatec Gmbh
FDA adverse event reports naming Altatec Gmbh as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: ALTATEC GMBH.
- Total reports
- 83,156
- Deaths
- 1
- Injuries
- 83,152
- Malfunctions
- 3
Reports per year
405
5207
1108
418
4019
52520
19,20221
12,15222
13,05723
16,35524
15,06425
6,69026
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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