FDAClass IIApril 1, 2020

Skytron Ergon 3 Series Skyboom Monitor recall

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

Why was Skytron Ergon 3 Series Skyboom Monitor 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.

What should I do if I have this product?

The recall is ongoing. Follow the firm and FDA instructions.

What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.

Is my product affected?

Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.

Which lot codes, UPCs or models are affected?

Serial Numbers: 1507T719-00-0-0087 1509T719-00-0-0142 1509T719-00-0-0144 1509T719-00-0-0139 1507T719-00-0-0085 1509T719-00-0-0135 1508T719-00-0-0115 1508T719-00-0-0116 1508T719-00-0-0119 1508T719-00-0-0120 1507T719-00-0-0074 1508T719-00-0-0129 1508T719-00-0-0121 1508T719-00-0-0123 1508T719-00-0-0124 1508T719-00-0-0125 1508T719-00-0-0126 1509T719-00-0-0132 1509T719-00-0-0146 1507T719-00-0-0103 1507T719-00-0-0104 1507T719-00-0-0053 1507T719-00-0-0054 1507T719-00-0-0055 1507T719-00-0-0056 1507T719-00-0-0058 1507T719-00-0-0059 1507T719-00-0-0061 1507T719-00-0-0062 1507T719-00-0-0063 1507T719-00-0-0064 1508T719-00-0-0127 1508T719-00-0-0128 1510T719-00-0-0153 1510T719-00-0-0154 1510T719-00-0-0157 1510T719-00-0-0160 1510T719-00-0-0166 1508T719-00-0-0118 1510T719-00-0-0159 1508T719-00-0-0114 1508T719-00-0-0117 1508T719-00-0-0122

Product
Skytron Ergon 3 Series Skyboom Monitor Bracket-Flatscreen Bracket, single monitor mount, 27" max. screen size Part number 3FCM1
Recalling firm
Skytron, Div. The KMW Group, Inc
Quantity
43 units
Distribution
AZ, CO, GA, IL, MI, MN, NJ, PA, VA, VT
Recall date
April 1, 2020
Classification
Class II
Status
Ongoing
Agency
FDA (device)
Open FDA enforcement record Latest recalls