MZIClass U
Test, Qualitative, For Hla, Non-Diagnostic
FDA adverse event reports and recall history for test, qualitative, for hla, non-diagnostic (product code MZI), from the public MAUDE/AEMS corpus and the live FDA recall database.
- Total reports
- 510
- Deaths
- 0
- Injuries
- 1
- Malfunctions
- 474
Reports per year
512
16213
20914
9715
616
2118
219
220
421
223
Source: FDA adverse event reports by year received, 2012–2023. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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