DRBClass 2
Stylet, Catheter
FDA adverse event reports and recall history for stylet, catheter (product code DRB), from the public MAUDE/AEMS corpus and the live FDA recall database.
- Total reports
- 1,267
- Deaths
- 76
- Injuries
- 1,001
- Malfunctions
- 186
Reports per year
4012
5313
6714
6615
5616
6317
4018
8219
9220
9721
9422
8223
11624
15425
7126
Source: FDA adverse event reports by year received, 2012–2026. 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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