KRHClass 2
Ring, Annuloplasty
FDA adverse event reports and recall history for ring, annuloplasty (product code KRH), from the public MAUDE/AEMS corpus and the live FDA recall database.
- Total reports
- 9,618
- Deaths
- 779
- Injuries
- 8,467
- Malfunctions
- 202
Reports per year
9012
9713
7314
14515
34716
37917
37818
34919
34020
42321
37222
32423
40724
42525
20926
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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