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Recall Observatory FDA recall evidence

Device evidence

device-recall:cfres:143569

CyberKnife Robotic; Catalog/part number 032000 and 033000 Cosmetic cover package. Product Usage: The CyberKnife Robotic Radiosurgery System is indicated for treatment planning and image guided stereotactic Radiosurgery and precision radiotherapy for lesions, tumors, and conditions anywhere in the body when radiation treatment is indicated.

Official recall number

Z-0771-2016

Evidence summary

Product code
IYE
Recall status
Terminated
Event initiated
January 22, 2016
Root cause
Device Design
Source snapshot
5482458777762b1480c71ac49b2913b9c7984bb55aac66a4315d018da7cfed2c
Product
Z-0771-2016

Field note

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