Synthes Hagendorf
FDA adverse event reports naming Synthes Hagendorf as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: SYNTHES HAGENDORF.
- Total reports
- 2,659
- Deaths
- 3
- Injuries
- 392
- Malfunctions
- 2,264
Reports per year
211
312
50514
72815
82216
59917
Source: FDA adverse event reports by year received, 2011–2017. Reporting paused twice in 2026 during FDA reporting-system changes and has since resumed.
Top device categories
- Orthopedic Manual Surgical InstrumentLXH791
- ScrewdriverHXX391
- Guide, Surgical, InstrumentFZX353
- Cerclage, FixationJDQ247
- Intervertebral Fusion Device With Bone Graft, LumbarMAX187
- Rod, Fixation, Intramedullary And AccessoriesHSB156
- TemplateHWT62
- ExtractorHWB58
- Intervertebral Fusion Device With Integrated Fixation, CervicalOVE57
- Prosthesis, Intervertebral DiscMJO56
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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