Recall Z-1309-2022— Skytron, Div. The KMW Group, Inc

Name: FDA recall Z-1309-2022
Creator: U.S. Food and Drug Administration
Published: 2022-06-02

Class II · Ongoing

Class II FDA medical device recall by Skytron, Div. The KMW Group, Inc, initiated 2022-06-02. FDA's recall record names no specific 510(k) clearance for this event. Product: Product Name: GCX Channel Mounting Accessory Model/Catalog Number: H8-300-40-A. Reason: 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..

Recalling firm: Skytron, Div. The KMW Group, Inc
Classification: Class II
Status: Ongoing
Initiated: 2022-06-02
Firm location: Grand Rapids, MI, United States

Product description

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.

Data sourced from openFDA. This site is unofficial and independent of the FDA.