# FDA recall Z-1569-2020

> **Skytron, Div. The KMW Group, Inc** · Class II · device recall initiated 2020-03-05.

## Product

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

## 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.

## Distribution

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

## Key facts

- **Recall number:** Z-1569-2020
- **Recalling firm:** Skytron, Div. The KMW Group, Inc
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2020-03-05
- **Report date:** 2020-04-01

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Grand Rapids, MI, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1569-2020

## Citation

> AI Analytics. FDA recall Z-1569-2020. Retrieved 2026-06-25 from https://api.ai-analytics.org/recall/Z-1569-2020. Source: US FDA. Licensed CC0.

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