Medical device recalls Moderate risk

Skytron, Div. The KMW Group, Inc recalls Ergon III Series Skyboom Monitor Bracket. Part # 3FCM1 Flatscreen Bracket, single monitor mount, 27inch max. screen size

Recall date
March 28, 2016
Source
U.S. Food & Drug Administration (FDA) — enforcement report
Recall number
Z-1871-2016
FDA classification
Class II
Brand / firm
Skytron, Div. The KMW Group, Inc
Sold / distributed
Worldwide distribution. US states: VA, VT, UT, GA, NJ, and IL; Japan.

Why it was recalled

Potential for the weld to fail at the pivot point of the monitor bracket. This weld failure could cause the display interface and bracket to fall from its mounted location, resulting in injury.

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

What was recalled

Ergon III Series Skyboom Monitor Bracket. Part # 3FCM1 Flatscreen Bracket, single monitor mount, 27inch max. screen size

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