Skytron, Div. The KMW Group, Inc: Medical Device Recall in 2020 - (Recall #: Z-0071-2021)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2020.

Data Source: FDA.

Product Description:

VGDF-SKY (R4-010-06) VGA TO FIBER CONVERTER-Single Format Faceplate, a component of the SkyVision Linx 300 Integration Control System Model: VGDF-SKY (version 2). For communication and visual image management in the operating room suite.

Product Classification:

Class II

Date Initiated: September 11, 2020

Date Posted: October 14, 2020

Recall Number: Z-0071-2021

Event ID: 86474

Reason for Recall:

VGDF (VGA) Faceplate failure results in failure of video signal for SkyVision Linx 300, a secondary display. Video would continue on the primary source device display

Status: Terminated

Product Quantity: 11 units

Code Information:

Serial Numbers: MXDM200501769 MXDM200501773 MXDM191100421 MXDM191100422 MXDM200200161 MXDM200200162 MXDM200200163 MXDM200200164 MXDM200501770 MXDM200501772 MXDM200501771

Distribution Pattern:

AZ, MI, MS, NJ, PA,

Voluntary or Mandated:

Voluntary: Firm initiated