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/AEMS corpus and the live FDA recall database.
- Total reports
- 10,394
- Deaths
- 6
- Injuries
- 100
- Malfunctions
- 10,003
Reports per year
58612
54213
52614
48515
62016
62617
68618
29819
7520
7621
7822
15123
6624
6625
2226
Source: FDA adverse event reports by year received, 2012–2026. 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.
Monitor system, test, automated blood grouping and antibody automatically
DeviceWatch watches FDA adverse events and recalls for the products you care about, summarizes clinical narratives with AI and alerts you when a safety signal emerges.