Siemens Medical Solutions USA, Inc recalls PRIMUS HI, Digital Linear Accelerator, Model No. 04504200
Recalled Product
PRIMUS HI, Digital Linear Accelerator, Model No. 04504200 Product Usage: The intended use of the device is to deliver x-ray radiation for therapeutic treatment of cancer.
Hazard / Issue
Control Console software has been updated to reduce the risk for collision when delivering automatically sequenced treatments with automatic movements of the gantry and/or the treatment table.
Issued by
FDA
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