FKJClass 2
Filter, Blood, Dialysis
FDA adverse event reports and recall history for filter, blood, dialysis (product code FKJ), from the public MAUDE/AEMS corpus and the live FDA recall database.
- Total reports
- 176
- Deaths
- 16
- Injuries
- 69
- Malfunctions
- 85
Reports per year
4900
1501
302
404
305
506
707
308
309
410
513
215
4816
1117
125
Source: FDA adverse event reports by year received, 2000–2025. 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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