Medical device recalls Moderate risk

Cook Inc. recalls Bentson Wire Guide

Recall date
October 13, 2017
Source
U.S. Food & Drug Administration (FDA) — enforcement report
Recall number
Z-0953-2018
FDA classification
Class II
Brand / firm
Cook Inc.
Sold / distributed
Nationally

Why it was recalled

Label does not state that the product is heparin-coated.

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

What was recalled

Bentson Wire Guide

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