Mindray DS USA, Inc. dba Mindray North America 2025-12-24 Health serious FDA
Health · FDA · Recall #FDA-Z-0920-2026
Hardware configuration of the BeneVision Central Monitoring System (CMS), marketed as… Recall
Issued December 24, 2025 · Mindray DS USA, Inc. dba Mindray North America
In December 2025, Mindray DS USA, Inc. dba Mindray North America recalled the Hardware configuration of the BeneVision Central Monitoring System (CMS), marketed as…, a serious health recall reported by the FDA.
Compiled by Maya Ellison, RecallCheckr
What this means for you
When the Worstation of the BeneVision DMS has a specific hardware configuration, the computer may experience audio playback failure or screen freezing.
What you should do
- 1 Stop using Hardware configuration of the BeneVision Central Monitoring System (CMS), marketed as… right away.
- 2 Set it aside where it won't be used by mistake.
- 3 Contact Mindray DS USA, Inc. dba Mindray North America to arrange your voluntary. See the official notice below for contact details.
- 4 Keep the product until your remedy is fully processed. You may need it.
Official remedy (Voluntary):
Recall details
- Brand
- Mindray DS USA, Inc. dba Mindray North America
- Category
- Health
- Recall date
- December 24, 2025
- Units affected
- Not reported
- Sold at
- Worldwide distribution - US Nationwide and the country of Canada.
- Recall number
- FDA-Z-0920-2026
- Made in
- United States
- Issuing agency
- FDA
In context
- Mindray DS USA, Inc. dba Mindray North America has 3 recalls in our database.
- We're tracking 3,576 Health recalls in our database.
- This is the 691st Health recall we've logged in 2025.