# FDA recall Z-1309-2022

> **Skytron, Div. The KMW Group, Inc** · Class II · device recall initiated 2022-06-02.

## Product

Product Name: GCX Channel Mounting Accessory  Model/Catalog Number: H8-300-40-A

## Reason for recall

Under certain circumstances, the mounting screws may loosen or pull out from the attachment point on the Ergon 3 boom when the GCX Channel Mounting Accessory was used with the VST clamp as a monitor mount on the boom.

## Distribution

Worldwide distribution - US Nationwide and the countries of Canada and Japan.

## Key facts

- **Recall number:** Z-1309-2022
- **Recalling firm:** Skytron, Div. The KMW Group, Inc
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2022-06-02
- **Report date:** 2022-07-06

- **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-1309-2022

## Citation

> AI Analytics. FDA recall Z-1309-2022. Retrieved 2026-06-25 from https://api.ai-analytics.org/recall/Z-1309-2022. Source: US FDA. Licensed CC0.

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