Sulzer Calcitek
FDA adverse event reports naming Sulzer Calcitek as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: SULZER CALCITEK.
- Total reports
- 1,472
- Deaths
- 0
- Injuries
- 1,468
- Malfunctions
- 0
Reports per year
32097
93998
21399
Source: FDA adverse event reports by year received, 1997–1999. 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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