Synthes Gmbh
FDA adverse event reports naming Synthes Gmbh as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: Synthes GmbH.
- Total reports
- 2,373
- Deaths
- 0
- Injuries
- 319
- Malfunctions
- 2,054
Top device categories
- Instrument, Surgical, Orthopedic, Ac-Powered Motor And Accessory/AttachmentHWE325
- Screw, Fixation, BoneHWC242
- ScrewdriverHXX226
- Plate, BoneJEY203
- Rod, Fixation, Intramedullary And AccessoriesHSB178
- Plate, Fixation, BoneHRS159
- Motor, Surgical Instrument, Ac-PoweredGEY157
- Orthopedic Manual Surgical InstrumentLXH136
- Bit, DrillHTW114
- ReamerHTO84
Recent recalls
No recalls listed in the FDA device recall database for this entry.
Monitor Synthes Gmbh 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.