Mindray DS USA, Inc. Recalls

1 recall found for Mindray DS USA, Inc.. Check if any of your products are affected.

HIGHFDA DEVICE

Mindray Recalls BeneVision N1 Patient Monitor Over Alarm Issues

Mindray DS USA, Inc. recalled 2,278 BeneVision N1 Patient Monitors on August 15, 2025. The monitors may activate an abnormal alarm pause, compromising patient safety. Health professionals must cease using these devices immediately and follow recall instructions.

Mindray DS USA, Inc.
Potential for
Read more

Brand Statistics

Total Recalls
1
Pages
1