Synthes Brandywine
FDA adverse event reports naming Synthes Brandywine as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: SYNTHES BRANDYWINE.
- Total reports
- 5,581
- Deaths
- 33
- Injuries
- 3,302
- Malfunctions
- 2,240
Reports per year
5408
13909
22710
30211
1,11412
1,39013
61214
91015
42816
38117
419
422
923
424
325
Source: FDA adverse event reports by year received, 2008–2025. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Top device categories
- Thoracolumbosacral Pedicle Screw SystemNKB1,476
- Prosthesis, Intervertebral DiscMJO1,364
- Orthopedic Manual Surgical InstrumentLXH376
- Guide, Surgical, InstrumentFZX373
- ScrewdriverHXX315
- Orthosis, Spondylolisthesis Spinal FixationMNH303
- Prosthesis, Rib ReplacementMDI291
- Appliance, Fixation, Spinal InterlaminalKWP209
- Gauge, DepthHTJ199
- Plate, Cranioplasty, Preformed, Non-AlterableGXN107
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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