Siemens Medical Solutions USA, Inc recalls PRIMUS, Accelerator, Linear, Medical The PRIMUSTM family of linear accelerator systems is to deliver x-ray radiation fo…

Recall date

July 26, 2016

Source

U.S. Food & Drug Administration (FDA) — enforcement report

Recall number

Z-2877-2016

FDA classification

Class II

Brand / firm

Siemens Medical Solutions USA, Inc

Sold / distributed

Nationwide distribution

Why it was recalled

Software patch installation to address several safety issues.

Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.

What was recalled

PRIMUS, Accelerator, Linear, Medical The PRIMUSTM family of linear accelerator systems is to deliver x-ray radiation for therapeutic treatment of cancer