Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-0071-2021 — 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.

U.S. FDA — Device Enforcement · United States · 2020-09-11 · Class II

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Agency: U.S. FDA — Device Enforcement
Recall identifier: Z-0071-2021
Date of alert: 2020-09-11
Country / jurisdiction: United States
Risk level: Class II
Risk type: recall
Brand: Skytron, Div. The KMW Group, Inc
Product category: device
Product type: Devices

Reported risk: 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

Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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ProductGuru indexes recall and safety-alert records from ~30 public agency registries. We are not lawyers, regulators or product-safety consultants. This page restates what the named agency published; consult the primary source above (or qualified counsel in your jurisdiction) before any commercial, medical or safety decision.

Recall Z-0071-2021 — 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.

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