Instrument, Surgical, Sonic And Accessory/Attachment
FDA adverse event reports and recall history for instrument, surgical, sonic and accessory/attachment (product code JDX), from the public MAUDE/AEMS corpus and the live FDA recall database.
- Total reports
- 173
- Deaths
- 0
- Injuries
- 84
- Malfunctions
- 87
Reports per year
Source: FDA adverse event reports by year received, 2009–2026. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Recent recalls
- TerminatedUnder Investigation by firm
Ultra-Drive Hose/Drape Assembly, Reference Number 423833 - Product Usage: Item used with the UltraDrive System to provide proper irrigation during the cutting and removal of bone and acrylic bone cement in orthopedic applications.
The products do not have sufficient data to support the labeled shelf life of 10 years.
- TerminatedUnder Investigation by firm
Ultra-Drive Irrigation Tubing Assembly, Reference Number 423834 - Product Usage: Item used with the UltraDrive System to provide proper irrigation during the cutting and removal of bone and acrylic bone cement in orthopedic applications.
The products do not have sufficient data to support the labeled shelf life of 10 years.
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