Official recall record
BeneVision N1 Patient Monitor
- Issuing authority
- Health Canada — Medical Devices
- Published
- 2025-08-28
- Country of alert
- Canada
- Alert level
- Type I
- Alert type
- recall
What the authority reported
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
What to do
Follow the instructions in the official notice — recall remedies (refund, repair, replacement, or disposal) are defined by the issuing authority and the responsible business, and they differ per recall. Do not rely on summaries, including this one.
Verify at the source:
Health Canada — Medical Devices — official record →
Record last checked against the registry on 2026-05-31.
Record last checked against the registry on 2026-05-31.
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