QHTClass U
Reagent Red Blood Cells
FDA adverse event reports and recall history for reagent red blood cells (product code QHT), from the public MAUDE/AEMS corpus and the live FDA recall database.
- Total reports
- 389
- Deaths
- 2
- Injuries
- 2
- Malfunctions
- 385
Reports per year
318
1419
8920
6021
4822
4523
5424
5125
2526
Source: FDA adverse event reports by year received, 2018–2026. 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.
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