Depuy Mitek LLC US
FDA adverse event reports naming Depuy Mitek LLC US as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: DEPUY MITEK LLC US.
- Total reports
- 24,400
- Deaths
- 0
- Injuries
- 2,167
- Malfunctions
- 22,233
Reports per year
613
115
716
4317
3,31018
3,51819
2,57120
2,55821
2,53022
3,00623
2,65424
2,61325
1,58326
Source: FDA adverse event reports by year received, 2013–2026. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Top device categories
- Fastener, Fixation, Biodegradable, Soft TissueMAI6,867
- ArthroscopeHRX5,206
- Electrosurgical, Cutting & Coagulation & AccessoriesGEI3,810
- Orthopedic Manual Surgical InstrumentLXH2,865
- Screw, Fixation, BoneHWC1,446
- Fastener, Fixation, Nondegradable, Soft TissueMBI837
- Accessories, ArthroscopicNBH828
- Staple, Fixation, BoneJDR440
- Cutter, SurgicalFZT410
- Applier, Staple, Surgical,GEF299
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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