KQSClass 1
Table, Cystometric, Non-Electric And Accessories
FDA adverse event reports and recall history for table, cystometric, non-electric and accessories (product code KQS), from the public MAUDE corpus and the live FDA recall database.
- Total reports
- 638
- Deaths
- 0
- Injuries
- 5
- Malfunctions
- 624
Reports per year
198
101
302
206
207
13808
17809
10610
17211
2112
213
114
116
220
122
Source: FDA adverse event reports by year received, 1998–2022. Reporting paused twice in 2026 during FDA reporting-system changes and has since resumed.
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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