KSJClass 3
System, Identification, Hepatitis B Antigen
FDA adverse event reports and recall history for system, identification, hepatitis b antigen (product code KSJ), from the public MAUDE/AEMS corpus and the live FDA recall database.
- Total reports
- 472
- Deaths
- 0
- Injuries
- 17
- Malfunctions
- 453
Reports per year
205
2307
408
4009
2210
2311
3712
2213
3214
1215
3016
7117
7918
6519
720
Source: FDA adverse event reports by year received, 2005–2020. 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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