Siemens Medical Solutions USA, Inc recalls Siemens LANTIS Oncology Information System Servers; allows the radiation therapist to deliver treatment to patient usin…

Recall date

January 21, 2015

Source

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

Recall number

Z-1282-2015

FDA classification

Class II

Brand / firm

Siemens Medical Solutions USA, Inc

Sold / distributed

Nationwide Distribution

Why it was recalled

There is a potential safety risk when using LANTIS server software with operating systems with which it has not been validated or released which can lead to an incorrect treatment to the patient.

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

What was recalled

Siemens LANTIS Oncology Information System Servers; allows the radiation therapist to deliver treatment to patient using the MEVATRON and all available accessories