JTAClass 1
Monitor, Microbial Growth
FDA adverse event reports and recall history for monitor, microbial growth (product code JTA), from the public MAUDE/AEMS corpus and the live FDA recall database.
- Total reports
- 108
- Deaths
- 9
- Injuries
- 31
- Malfunctions
- 56
Reports per year
1108
409
310
211
212
213
114
116
118
419
521
122
123
325
226
Source: FDA adverse event reports by year received, 2008–2026. 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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