VGDF-SKY — Class II medical device recall Z-0071-2021
Terminated recall by Skytron, Div. The KMW Group, Inc, reported 2020-10-14, distributed in AZ, MI, MS, NJ, PA. VGDF (VGA) Faceplate failure results in failure of video signal for SkyVision Linx 300, a secondary display. V
| Recall number | Z-0071-2021 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Skytron, Div. The KMW Group, Inc, Grand Rapids, MI, United States |
| Recall initiated | 2020-09-11 |
| Classified | 2020-10-08 |
| Reported by FDA | 2020-10-14 |
| Terminated | 2024-09-24 |
| Distributed | AZ, MI, MS, NJ, PA |
| Quantity | 11 units |
| Serial numbers | MXDM191100421, MXDM191100422, MXDM200200161, MXDM200200162, MXDM200200163, MXDM200200164, MXDM200501769, MXDM200501770, MXDM200501771, MXDM200501772, MXDM200501773 |
Product
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.
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
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-0071-2021. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.