Medical device recalls Moderate risk

Skytron, Div. The KMW Group, Inc recalls Skytron Ergon 3 Series Skyboom Monitor Bracket-Flatscreen Bracket, single monitor mount, 27" max. screen size Part numb…

Recall date
March 5, 2020
Source
U.S. Food & Drug Administration (FDA) — enforcement report
Recall number
Z-1569-2020
FDA classification
Class II
Brand / firm
Skytron, Div. The KMW Group, Inc
Sold / distributed
AZ, CO, GA, IL, MI, MN, NJ, PA, VA, VT

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

Skytron Ergon 3 Series Skyboom Monitor Bracket-Flatscreen Bracket, single monitor mount, 27" max. screen size Part number 3FCM1

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