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Benevision n1 patient monitor
Official notice
28 Aug 2025
Last checked
28 Aug 2025
An official Health Canada notice concerns Benevision n1 patient monitor. Mindray has identified that, under rare circumstances, using the BeneVision N1 Patient Monitor with software versions 01.60.00.01 and 01.61.00.01 as a multi-parameter module in conjunction with a host monitor may result in the activation of an abnormal alarm pause. This can occur if the alarm pause button is pressed twice rapidly on either the N1 or the host monitor. Recall start date: August 19, 2025 Published 2025-08-28.
What to do now
Contact the manufacturer if you require additional information.
Recall number
77995
Official notice
2025-08-28
The hazard
The hazard
Mindray has identified that, under rare circumstances, using the BeneVision N1 Patient Monitor with software versions 01.60.00.01 and 01.61.00.01 as a multi-parameter module in conjunction with a host monitor may result in the activation of an abnormal alarm pause. This can occur if the alarm pause button is pressed twice rapidly on either the N1 or the host monitor. Recall start date: August 19, 2025
How to check if you're affected
How to check if you're affected
Compare the product name and identifiers below with the item you own. Follow the official notice if they match.
Recall Numbers
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Affected products
Product 1
Risk / hazard
Where it was sold
Where it was sold
The source does not list specific retailers. See the official notice for where affected products were sold.
Location 1
Affected area 1
Company & contacts
Company & contacts
Manufacturer
Phone
Brand: Shenzhen Mindray Bio-medical Electronics, Benevision N1 Patient Monitor.
Source & status
Source & status
Source
Tier
Category
Classification
App estimate
Recall details
Recall details
Recall number
Classification
Source tier
Documents, notices & source
See the official notice and source documents for full details.
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