PlainRecalls
FDA Devices Moderate Class II Terminated

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).

Reported: April 19, 2017 Initiated: March 13, 2017 #Z-1768-2017

Product Description

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).

Reason for Recall

The Pause function on central monitors will not automatically resume when connected to a Life Scope G9 patient monitor.

Details

Recalling Firm
Nihon Kohden America Inc
Units Affected
654 units total (230 units in US)
Distribution
Worldwide - US Nationwide Distribution including the countries of Germany, Spain, Brazil, Paraguay, Bolivia, Chile, Colombia, Costa Rica, Mexico, Peru, Pakistan, Israel, Qatar, Saudi Arabia, South Africa, Tunisia, United Arab Emirates, Korea, Malaysia, Singapore, Thailand
Location
Irvine, CA

Frequently Asked Questions

What product was recalled?
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).. Recalled by Nihon Kohden America Inc. Units affected: 654 units total (230 units in US).
Why was this product recalled?
The Pause function on central monitors will not automatically resume when connected to a Life Scope G9 patient monitor.
Which agency issued this recall?
This recall was issued by the FDA Devices on April 19, 2017. Severity: Moderate. Recall number: Z-1768-2017.