LQYClass U
Locator, Root Apex
FDA adverse event reports and recall history for locator, root apex (product code LQY), from the public MAUDE/AEMS corpus and the live FDA recall database.
- Total reports
- 1,402
- Deaths
- 0
- Injuries
- 9
- Malfunctions
- 1,393
Reports per year
14011
5912
213
5915
12816
13317
15418
16319
13920
10721
6322
5623
8124
5225
2826
Source: FDA adverse event reports by year received, 2011–2026. 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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