Synthes Mezzovico
FDA adverse event reports naming Synthes Mezzovico as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: SYNTHES MEZZOVICO.
- Total reports
- 1,119
- Deaths
- 5
- Injuries
- 778
- Malfunctions
- 336
Reports per year
113
25514
29715
28216
28417
Source: FDA adverse event reports by year received, 2013–2017. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Top device categories
- Thoracolumbosacral Pedicle Screw SystemNKB216
- Plate, Fixation, BoneHRS210
- Condylar Plate Fixation ImplantJDP146
- Screw, Fixation, BoneHWC114
- Intervertebral Fusion Device With Integrated Fixation, CervicalOVE89
- Plate, Cranioplasty, Preformed, Non-AlterableGXN45
- Appliance, Fixation, Spinal Intervertebral BodyKWQ41
- Rod, Fixation, Intramedullary And AccessoriesHSB38
- Plate, BoneJEY29
- Appliance, Fixation, Spinal InterlaminalKWP29
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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