Medical device recalls Moderate risk

Siemens Medical Solutions USA, Inc recalls SOMATOM Definition AS system, x-ray, tomography, computed

Recall date
October 19, 2016
Source
U.S. Food & Drug Administration (FDA) — enforcement report
Recall number
Z-0373-2017
FDA classification
Class II
Brand / firm
Siemens Medical Solutions USA, Inc
Sold / distributed
Nationwide Distribution

Why it was recalled

Hardware issue that may expose the User to a potential risk for serious injury due to exposure to rotating or electrical parts.

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

What was recalled

SOMATOM Definition AS system, x-ray, tomography, computed

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