Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
BSM-3000 Series Bedside Monitor REF BSM-3572A The Life Scope BSM-3000 Recalled by Nihon Kohden America Inc Due to Due to software issue the device may give...
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 Nihon Kohden America Inc directly.
Affected Products
BSM-3000 Series Bedside Monitor REF BSM-3572A The Life Scope BSM-3000 Series Bedside Monitoring System is intended to monitor, display and record physiological data to provide cardiac and vital signs monitoring within a medical facility.
Quantity: 16 systems
Why Was This Recalled?
Due to software issue the device may give false "SpO2 Probe Failure" alarm
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Nihon Kohden America Inc
Nihon Kohden America Inc has 10 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report