Synthes Selzach
FDA adverse event reports naming Synthes Selzach as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: SYNTHES SELZACH.
- Total reports
- 1,392
- Deaths
- 1
- Injuries
- 548
- Malfunctions
- 843
Reports per year
22714
34715
37016
44817
Source: FDA adverse event reports by year received, 2014–2017. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Top device categories
- Plate, Fixation, BoneHRS200
- Bit, DrillHTW156
- Instrument, Surgical, Orthopedic, Ac-Powered Motor And Accessory/AttachmentHWE130
- Screw, Fixation, BoneHWC106
- Cement, Bone, VertebroplastyNDN99
- ReamerHTO98
- Drill, Bone, PoweredDZI63
- Nail, Fixation, BoneJDS62
- Rod, Fixation, Intramedullary And AccessoriesHSB55
- ForcepsHTD50
Recent recalls
No recalls listed in the FDA device recall database for this entry.
Monitor Synthes Selzach 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.