Stryker Osteosynthesis Freiburg
FDA adverse event reports naming Stryker Osteosynthesis Freiburg as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: STRYKER OSTEOSYNTHESIS FREIBURG.
- Total reports
- 1,338
- Deaths
- 0
- Injuries
- 183
- Malfunctions
- 1,061
Reports per year
3707
5808
19809
41610
35911
25112
1913
Source: FDA adverse event reports by year received, 2007–2013. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Top device categories
- Plate, BoneJEY363
- Orthopedic Manual Surgical InstrumentLXH326
- Plate, Fixation, BoneHRS298
- ScrewdriverHXX80
- Screw, Fixation, BoneHWC65
- Drills, Burrs, Trephines & Accessories (Simple, Powered)HBE63
- Bit, DrillHTW13
- Electrosurgical, Cutting & Coagulation & AccessoriesGEI11
- Instrument, Surgical, Orthopedic, Dc-Powered Motor And Accessory/AttachmentKIJ10
- Screw, Fixation, IntraosseousDZL8
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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