FDANovember 22, 2016device

CyberKnife Robotic Radiosurgery System using software version 10.6; Catalog/Part Number: 54000 UDI: M658053301 0 Radiology: The CyberKnife Robotic Radiosurgery System is indicated for treatment planning and image guided stereotactic Radiosurgery and precision radiotherapy for lesions, tumors and ...

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

Accuray has become aware of a potential safety issue involving unexpected treatment robot motion when removing an accessory. This issue is limited to certain CyberKnife¿ Systems with software version 1 0.6.

What to do

FDA enforcement status: Terminated

Brands named

accuray

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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