Mindray recalls BeneVision Distributed Monitoring hardware with audio driver version 6.0.9484.1 due to possible audio playback failure or screen freezing. Affected units include specific HP Pro Mini 400 G9 models.
When the Worstation of the BeneVision DMS has a specific hardware configuration, the computer may experience audio playback failure or screen freezing.
Mindray is recalling certain BeneVision Distributed Monitoring systems that may experience audio playback failure or screen freezing. This could disrupt medical monitoring during use, requiring immediate attention to ensure patient safety.
The system may experience audio playback failure or screen freezing when the specific hardware configuration is active. This could disrupt critical medical monitoring signals, potentially delaying patient care.
Healthcare providers using the BeneVision Distributed Monitoring system with the specific hardware configuration are most at risk. Patients being monitored by this equipment could be affected if the system malfunctions.
Check for the model number 115-050935-00 or E115-050935-00 on the hardware. The affected units include HP Pro Mini 400 G9 Desktop PCs with audio driver version 6.0.9484.1.
Verify if your BeneVision Distributed Monitoring system has the model numbers 115-050935-00 or E115-050935-00.
The recall involves specific hardware configurations with the model numbers 115-050935-00 and E115-050935-00, including HP Pro Mini 400 G9 Desktop PCs with audio driver version 6.0.9484.1.
Check for the model numbers 115-050935-00 or E115-050935-00 on the hardware. Affected units include HP Pro Mini 400 G9 Desktop PCs with audio driver version 6.0.9484.1.
The recall does not specify a remedy, so contact Mindray for further instructions.
We’ve drafted a message you can send Mindray to request your refund or repair — edit it as you like.
Subject: Recall Z-0920-2026 — Mindray Mindray Hello, I own a Mindray that is covered by recall Z-0920-2026 from Mindray. 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.
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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.
