Stryker Leibinger Freiburg
FDA adverse event reports naming Stryker Leibinger Freiburg as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: STRYKER LEIBINGER FREIBURG.
- Total reports
- 2,069
- Deaths
- 0
- Injuries
- 777
- Malfunctions
- 1,290
Reports per year
210
8313
28314
24415
29016
29717
9818
5919
5720
4821
3822
8823
11924
14425
10726
Source: FDA adverse event reports by year received, 2010–2026. Reporting paused twice in 2026 during FDA reporting-system changes and has since resumed.
Top device categories
- Plate, BoneJEY633
- Plate, Fixation, BoneHRS426
- Orthopedic Manual Surgical InstrumentLXH281
- Plate, Cranioplasty, Preformed, AlterableGWO157
- Orthopedic Stereotaxic InstrumentOLO80
- Neurological Stereotaxic InstrumentHAW78
- Drills, Burrs, Trephines & Accessories (Simple, Powered)HBE61
- Screw, Fixation, BoneHWC50
- Bit, DrillHTW44
- Screw, Fixation, IntraosseousDZL36
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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