Health ProductsType I recall

BeneVision N1 Patient Monitor

· Published by Health Canada · Official notice

Details

Alert type: Health product recall
Category: Health products - Medical devices - Cardiovascular
Product: BeneVision N1 Patient Monitor
Issue: Medical devices - Performance
What to do: Contact the manufacturer if you require additional information.
Audience: Healthcare
Recall class: Type I
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Products

Affected productsLot or serial numberModel or catalogue number
BeneVision N1 Patient MonitorMore 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

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