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Open, Classified

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

FDA Recall Z-1569-2020 · Posted None

Recalling FirmSkytron, Div. The KMW Group, Inc
Recall StatusOpen, Classified
Product CodeFQO
Date Initiated2020-03-05
Product Quantity43 units

Reason for Recall

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.

Firm Action

Skytron customer notification letters mailed on 3/5/2020. Distributors received notification via email on 3/5/2020. Letter states reason for recall, health risk and action to take: 1.Identify and inspect your 3FCM1 monitor bracket(s). 1508T719-00-0-0120 2.Remove from service any bracket with noticeable physical distortion or cracking around the welded area. 3.Skytron authorized representatives have been directed to contact and schedule a service visit within a 30-day window of time. The contact information for your authorized representative is: Johnsons Medical, Inc. Donna Johnson, (801) 768-4411 Please contact Erin Woolf, at 616-656-2998 or [email protected] with any questions. For after-hours support, please call 1-800-SKYTRON.

Root Cause

Device Design

Distribution Pattern

AZ, CO, GA, IL, MI, MN, NJ, PA, VA, VT

Related FDA 510(k) Records

Devices referenced by this recall via K-numbers.

K950192SKYTRON SKYBOOM SERIESSkytron, Div. the Kmw Group, Inc. · 1995-04-03

Official Source

View FDA Recall →

Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.

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