Day

June 6, 2024
06
Jun

FDA Recall: Device May Give False “SpO2 Probe Failure” Alarm

June 6, 2024
Company: Nihon Kohden America Inc Date of Enforcement Report: 6/6/2024 Class II 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 Recall Number: Z-2025-2024 REASON: Due to software issue...
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