FDAMarch 13, 2017device
Bedside monitor CSM-1901(Life Scope G9) with main unit CU-192RA. The Problem only affects CSM-1901(Life Scope G9) communicating with CNS-6201A (PU-621RA) and CNS-9701A (MU-971RA).
Official recall recorded by the U.S. Food & Drug Administration.
The hazard
The Pause function on central monitors will not automatically resume when connected to a Life Scope G9 patient monitor.
What to do
FDA enforcement status: Terminated
Brands named
nihon kohden americanihonnihon kohden
Recall history
Other federal recalls tied to the same brand — a factual pattern, straight from the source data.
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- FDADigitalDiagnost C90 Flex/Value/Chest/ER. Model Number: 712035.2026-05-01
- CPSCAcer America Corporation Recalls Two-Wheeled Folding Electric Due to Risk of Injury from Fall Hazard2026-04-30
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