Synthes Oberdorf
FDA adverse event reports naming Synthes Oberdorf as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: SYNTHES OBERDORF.
- Total reports
- 8,191
- Deaths
- 0
- Injuries
- 64
- Malfunctions
- 8,126
Reports per year
1911
112
113
87214
2,17015
2,94816
2,17217
818
Source: FDA adverse event reports by year received, 2011–2018. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Top device categories
- Instrument, Surgical, Orthopedic, Ac-Powered Motor And Accessory/AttachmentHWE4,823
- Motor, Surgical Instrument, Ac-PoweredGEY2,385
- Battery, Replacement, RechargeableMOQ621
- Blade, Saw, General & Plastic Surgery, SurgicalGFA108
- Motor, Drill, PneumaticHBB44
- Plate, BoneJEY35
- Instrument, Surgical, Orthopedic, Pneumatic Powered & Accessory/AttachmentHSZ18
- Orthopedic Manual Surgical InstrumentLXH17
- Tray, Surgical, InstrumentFSM12
- Filler, Bone Void, Calcium CompoundMQV12
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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