KSZClass 2
System, Test, Automated Blood Grouping And Antibody
FDA adverse event reports and recall history for system, test, automated blood grouping and antibody (product code KSZ), from the public MAUDE corpus and the live FDA recall database.
- Total reports
- 10,401
- Deaths
- 6
- Injuries
- 100
- Malfunctions
- 10,010
Reports per year
58612
54213
52614
48515
62016
62617
68618
29819
7520
7621
7822
15123
6624
6625
2826
Source: FDA adverse event reports by year received, 2012–2026. 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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