BeneVision N1 Patient Monitor
Last updated
Summary
Product
BeneVision N1 Patient Monitor
Issue
Medical devices - Performance
What to do
Contact the manufacturer if you require additional information.
Audience
Healthcare
Affected products
| Affected products | Lot or serial number | Model or catalogue number |
|---|---|---|
| BeneVision N1 Patient Monitor | More than 10 numbers, contact manufacturer. | BENEVISION N1 |
Issue
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
Additional information
Details
Original published date:
Alert / recall type
Health product recall
Category
Health products - Medical devices - Cardiovascular
Companies
Shenzhen Mindray Bio-Medical Electronics Co., Ltd.
Mindray Building, Suite 3b, Shenzhen, Guangdong, China, 518057
Published by
Health Canada
Audience
Healthcare
Recall class
Type I
Identification number
RA-77995
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