Spacelabs recalls Xhibit Central Station Model 96102 due to audio/video failures in the DisplayPort splitter component. Affected units may show distorted or no video output.
Due to off-the-shelf display port component that has audio/video failures
Spacelabs is recalling Xhibit Central Station Model 96102 because a third-party DisplayPort splitter component has audio/video failures. This could cause distorted or no video output on connected monitors, but does not affect patient safety directly.
The DisplayPort audio/video splitter (a third-party accessory) has audio/video failures. This means connected external displays may show distorted or no video output, but the device does not interact with patient data or pose a safety risk.
Healthcare facilities using Spacelabs Xhibit Central Station Model 96102 for patient monitoring systems. Staff who connect external displays to this unit are most at risk.
Check for the model number 96102 on the Xhibit Central Station. The DisplayPort splitter part number is 010-1975-00. Units sold with this model number are affected.
Inspect the DisplayPort splitter for audio/video failures. If displays show distorted or no video, stop using the splitter.
No, the recall is for audio/video display failures only. The device does not interact with patient data or pose a safety risk.
Check for model number 96102 on the Xhibit Central Station. The DisplayPort splitter part number is 010-1975-00.
The recall does not provide a fix. Affected units may need to replace the DisplayPort splitter if audio/video fails.
We’ve drafted a message you can send Spacelabs to request your refund or repair — edit it as you like.
Subject: Recall Z-2916-2026 — Spacelabs Spacelabs Hello, I own a Spacelabs that is covered by recall Z-2916-2026 from Spacelabs. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.