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
- 2,040
- Deaths
- 0
- Injuries
- 755
- Malfunctions
- 1,283
Reports per year
210
8313
28314
24415
29016
29717
9818
5919
5720
4821
3822
8823
11924
14425
7826
Source: FDA adverse event reports by year received, 2010–2026. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Top device categories
- Plate, BoneJEY632
- Plate, Fixation, BoneHRS412
- Orthopedic Manual Surgical InstrumentLXH281
- Plate, Cranioplasty, Preformed, AlterableGWO157
- Neurological Stereotaxic InstrumentHAW75
- Orthopedic Stereotaxic InstrumentOLO74
- Drills, Burrs, Trephines & Accessories (Simple, Powered)HBE61
- Screw, Fixation, BoneHWC50
- Bit, DrillHTW44
- Screw, Fixation, IntraosseousDZL31
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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