Medical device recalls Moderate risk

Craftmatic Industries, Inc. recalls Craftmatic Model 1 Base for Dual Bed Configurations

Recall date
March 24, 2017
Source
U.S. Food & Drug Administration (FDA) — enforcement report
Recall number
Z-1499-2022
FDA classification
Class II
Brand / firm
Craftmatic Industries, Inc.
Sold / distributed
US Nationwide distribution - product was not distributed outside of the United States

Why it was recalled

A potential for dual-configured beds to separate or slip away from one another.

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

What was recalled

Craftmatic Model 1 Base for Dual Bed Configurations

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