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.
Take action
Contact the company
📍Recalling firmMindray DS USA, Inc. dba Mindray North America800 Macarthur Blvd · Mahwah, NJ 07430-2001
“Mindray BeneVision Distributed Monitoring: Audio Failure Risk.” GovInfoNow, updated August 18, 2026. https://govinfonow.com/recall/50640-mindray-benevision-distributed-monitoring-audio-failure-risk. Based on FDA recall #Z-0920-2026 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0920-2026%22&limit=1).
Mindray DS USA, Inc. dba Mindray North America recalled the BeneVision Central Monitoring System hardware configuration due to potential audio playback failure or screen freezing, according to a Food and Drug Administration announcement on Nov. 18, 2025.
How to tell if you have it
BeneVision Distributed Monitoring System
Model Number: 115-050935-00
Model Number: E115-050935-00
UDI-DI: 06936415972417
HP Pro Mini 400 G9 Desktop PC with Realtek HD Audio Driver Officially Released by HP (audio driver version 6.0.9484.1)
Audio Driver Version: 6.0.9484.1
The hazard
When the Worstation of the BeneVision DMS has a specific hardware configuration, the computer may experience audio playback failure or screen freezing.
Context
GovInfoNow's records show Mindray DS USA, Inc. dba Mindray North America has 13 other recalls on record since 2017-07-14. Other recent recalls of similar products include Mindray Isoflurane V90 Vaporizer Recall (2025-10-20), Mindray BeneVision N1 Patient Monitor Recall (2025-08-15), and Mindray Sevoflurane E_Vap Quik-Fil Recall (2024-07-22).
How to tell if you have this one
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.
Brand
Mindray
Category
Medical device
Based on the official FDA remedy
What to do — step by step
Check Hardware Configuration
Verify if your BeneVision Distributed Monitoring system has the model numbers 115-050935-00 or E115-050935-00.
Where it went and when
Where it was distributed
Distributed nationwide, and outside the U.S.
Nationwide
Not listed
FDA distribution: “Worldwide distribution - US Nationwide and the country of Canada.” States read from FDA’s own wording; “not listed” means the notice does not name it.
Distributed nationwide, and outside the U.S.
Recall timeline
FDA published this recall 36 days after the firm started it.
1Firm started the recall
2FDA classified it Class II
3Published in FDA’s Enforcement Report
Dates from the agency record only; steps without a date are left out.
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.
Official source: FDA Recall #Z-0920-2026 (November 18, 2025) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-0920-2026 to see it in context.
Plain-language summary written by qwen3:4b on August 18, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.