JESClass 1
Floss, Dental
FDA adverse event reports and recall history for floss, dental (product code JES), from the public MAUDE/AEMS corpus and the live FDA recall database.
- Total reports
- 649
- Deaths
- 0
- Injuries
- 197
- Malfunctions
- 429
Reports per year
9812
7513
8414
4515
4316
5017
5218
5219
3220
3221
822
323
624
525
126
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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