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
- 78,929
- Deaths
- 44
- Injuries
- 20,555
- Malfunctions
- 58,322
Reports per year
35611
1,71912
6,10813
1,74914
115
116
818
919
1,36120
9,90721
10,97122
14,07023
13,54624
12,56725
6,55426
Source: FDA adverse event reports by year received, 2011–2026. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Top device categories
- Instrument, Surgical, Orthopedic, Ac-Powered Motor And Accessory/AttachmentHWE13,348
- Screw, Fixation, BoneHWC10,163
- Rod, Fixation, Intramedullary And AccessoriesHSB6,065
- Motor, Surgical Instrument, Ac-PoweredGEY5,050
- Plate, Fixation, BoneHRS4,642
- ScrewdriverHXX4,363
- Orthopedic Manual Surgical InstrumentLXH4,189
- Plate, BoneJEY3,076
- Bit, DrillHTW3,066
- Guide, Surgical, InstrumentFZX2,665
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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