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 during the 2026 MAUDE-to-AEMS transition 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.
Monitor Synthes Hagendorf automatically
DeviceWatch watches FDA adverse events and recalls for the products you care about, summarizes clinical narratives with AI and alerts you when a safety signal emerges.