PJEClass 2
Blood/Plasma Collection Device For Dna Testing
FDA adverse event reports and recall history for blood/plasma collection device for dna testing (product code PJE), from the public MAUDE/AEMS corpus and the live FDA recall database.
- Total reports
- 580
- Deaths
- 0
- Injuries
- 0
- Malfunctions
- 580
Reports per year
2718
1219
320
1421
1622
6323
16824
26425
1326
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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