Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
BeneVision N1 Patient Monitor (N1). Part Numbers: 6660E-PA00017 Recalled by Mindray DS USA, Inc. dba Mindray North America Due to Potential for activation of an abnormal alarm pause.
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Mindray DS USA, Inc. dba Mindray North America directly.
Affected Products
BeneVision N1 Patient Monitor (N1). Part Numbers: 6660E-PA00017, 6660E-PA00014, 6660E-PA00012, 6660E-PA00011, 6660E-PA00018, 6660E-PA00015, 6660E-PA00020, Q6660E-PA00011, 6660E-PA00021, 6660E-PA00016, 6660E-PA00019, Q6660E-PA00018, 6660E-PA00010, Q6660E-PA00010, Q6660E-PA00021, Q6660E-PA00012, 6660E-PA00030, 6660E-PA00041, 6660E-PA00035, 6660E-PA00032, 6660E-PA00031. Software Versions: 1.04.00.01, 01.05.00.01, 01.06.00.01, and 01.06.01.01 The patient monitor is intended for monitoring, displaying, reviewing, storing, alarming and transferring of multiple physiological parameters.
Quantity: 2,278 units
Why Was This Recalled?
Potential for activation of an abnormal alarm pause.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Mindray DS USA, Inc. dba Mindray North America
Mindray DS USA, Inc. dba Mindray North America has 39 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report