MZMClass 2
Fibrin Sealant Preparation Device
FDA adverse event reports and recall history for fibrin sealant preparation device (product code MZM), from the public MAUDE corpus and the live FDA recall database.
- Total reports
- 419
- Deaths
- 3
- Injuries
- 1
- Malfunctions
- 413
Reports per year
107
111
216
417
619
3820
2621
10322
4723
8224
8125
2826
Source: FDA adverse event reports by year received, 2007–2026. Reporting paused twice in 2026 during FDA reporting-system changes and has since resumed.
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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