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Viewray Incorporated recalls Patient Handling System (Motion Control Software), Product Usage: Indicated for stereotactic radiosurgery and preci
Recalled July 22, 2015 · FDA recall Z-2085-2015 · Viewray Incorporated
Hazard
ViewRay received a report that the couch moved unexpectedly into the bore after performing a RTCS reboot. · FDA Class II
Units
3
Sold at
US Nationwide Distribution in the states of CA, MO & WI
Description
ViewRay received a report that the couch moved unexpectedly into the bore after performing a RTCS reboot.
Product
Patient Handling System (Motion Control Software), Product Usage: Indicated for stereotactic radiosurgery and precision radiotherapy for lesions, tumors, and conditions anywhere in the body when radiation treatment is indicated.
Manufacturer(s)
Viewray Incorporated
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →