Accuray Incorporated recalls Cyberknife Treatment Deliver System equipped with the Xchang
See all recalls from Accuray Incorporated →Recalled Product
Cyberknife Treatment Deliver System equipped with the Xchange Robotic Collimator Changer; Linear Accelerator
Hazard / Issue
In certain cases, a collimator may not fully dock, which triggers a system interlock and prevents motion from the operator console. If personnel then enter the treatment room and initiate motion using the in-room control pendant, the collimator may release and fall from the housing.
Issued by
FDA
Distribution: Nationwide (United States)
Lot/Code Info: All systems prior with software version 11X that utilize the Exchange Table
✅ What Should You Do?
- 1Contact your healthcare provider immediately to discuss this recall.
- 2Stop using the device if it is safe to do so, and contact your provider.
- 3Follow the manufacturer's remedy instructions provided in the recall notice.
- 4Report device problems to FDA MedWatch or call 1-800-FDA-1088.
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