Nihon Kohden America Inc recalls BSM-3000 Series Bedside Monitor REF BSM-3572A The Life Scope BSM-3000 Series Bedside Monitoring System is intended to

Recalled June 12, 2024 · FDA recall Z-2025-2024 · Nihon Kohden America

Hazard

Due to software issue the device may give false "SpO2 Probe Failure" alarm · FDA Class II

Units

16 systems

Sold at

U.S. Nationwide distribution in the state of IA.

Description

Due to software issue the device may give false "SpO2 Probe Failure" alarm

Product

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.

Manufacturer(s)

Nihon Kohden America Inc

Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →