Health & Personal Care
HIGH
FDA DEVICE
Mindray BeneVision N1 Patient Monitor Recall Issued for 2,278 Units Worldwide (2025)
Mindray DS USA, Inc. dba Mindray North America recalled 2,278 BeneVision N1 patient monitors distributed worldwide, including Canada. The devices may activate an abnormal alarm pause. Hospitals and clinicians should stop using the devices immediately and follow the recall instructions issued by Mindray.
Mindray
Potential for