FJGClass 2
Dialyzer, Parallel Flow
FDA adverse event reports and recall history for dialyzer, parallel flow (product code FJG), from the public MAUDE/AEMS corpus and the live FDA recall database.
- Total reports
- 101
- Deaths
- 1
- Injuries
- 46
- Malfunctions
- 40
Reports per year
293
194
395
6596
597
698
1799
200
Source: FDA adverse event reports by year received, 1993–2000. 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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