GKJClass 1
Spinner, Slide, Automated
FDA adverse event reports and recall history for spinner, slide, automated (product code GKJ), from the public MAUDE/AEMS corpus and the live FDA recall database.
- Total reports
- 105
- Deaths
- 0
- Injuries
- 4
- Malfunctions
- 101
Reports per year
197
108
209
310
2311
6612
513
115
116
118
119
Source: FDA adverse event reports by year received, 1997–2019. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Recent recalls
- 2006-02-04TerminatedOther
COULTER GEN.S Series Hematology Analyzer, PN 6605632, 6605632R; GENS: 6605381, 6605381R, 6605360, 6605360R, 6605470, 6605470R
There is a risk of sample misidentification when processing samples in the Manual aspiration mode.
Monitor spinner, slide, automated automatically
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