EMRClass 1
File, Periodontic
FDA adverse event reports and recall history for file, periodontic (product code EMR), from the public MAUDE corpus and the live FDA recall database.
- Total reports
- 105
- Deaths
- 0
- Injuries
- 3
- Malfunctions
- 102
Reports per year
502
5303
1704
1905
906
223
Source: FDA adverse event reports by year received, 2002–2023. 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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