Synthes Bettlach
FDA adverse event reports naming Synthes Bettlach as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: SYNTHES BETTLACH.
- Total reports
- 2,758
- Deaths
- 1
- Injuries
- 969
- Malfunctions
- 1,788
Reports per year
611
65114
83315
63716
62917
218
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
- Rod, Fixation, Intramedullary And AccessoriesHSB513
- Bit, DrillHTW319
- Guide, Surgical, InstrumentFZX248
- Orthopedic Manual Surgical InstrumentLXH240
- Appliance, Fixation, Nail/Blade/Plate Combination, Multiple ComponentKTT238
- ReamerHTO164
- Instrument, Surgical, Orthopedic, Ac-Powered Motor And Accessory/AttachmentHWE113
- ImpactorHWA108
- ScrewdriverHXX96
- ExtractorHWB93
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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