Medical device recalls Moderate risk

Deerfield Imaging recalls IMRIS DEERFIELD IMAGING, REF 113803, Starburst adaptor thumb screw

Recall date
August 14, 2017
Source
U.S. Food & Drug Administration (FDA) — enforcement report
Recall number
Z-3211-2017
FDA classification
Class II
Brand / firm
Deerfield Imaging
Sold / distributed
IL, OR, PA

Why it was recalled

incorrect thread on thumbscrews

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

What was recalled

IMRIS DEERFIELD IMAGING, REF 113803, Starburst adaptor thumb screw

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