KZLClass 2
Device, Warming. Blood And Plasma
FDA adverse event reports and recall history for device, warming. blood and plasma (product code KZL), from the public MAUDE corpus and the live FDA recall database.
- Total reports
- 828
- Deaths
- 8
- Injuries
- 14
- Malfunctions
- 805
Reports per year
1412
4213
2514
1615
1016
517
318
219
5320
7121
10222
10623
5724
7825
3726
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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