Reported Jul 9, 2014 · Terminated

CNS-6200 Series Central Nurse Station and accessories. Model Number: CNS-6201 For cardiac and vital signs monitoring…

Nihon Kohden America Inc.

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: Nihon Kohden America Inc · 15353 Barranca Pkwy · Irvine, CA · 92618-2216

Is this the product you have?

  • CNS-6200 Series Central Nurse Station and accessories
  • Model NumberCNS-6201 For cardiac and vital signs monitoring for multiple patients
Lot codes and dates
  • Model NumberCNS-6201 Software Version 02-26 only
  • Serial Numbers
    • 00485
    • 00488
    • 00489
    • 00490
    • 00491
    • 00361
    • 00429
    • 00430
    • 00432
    • 00436
    • 00443
    • 00447
    • 00478
    • 00486
    • 00546
    • 00564
    • 00573
    • 00574
    • 00575
    • 00576
    • 00592
    • 00626
    • 00638
    • 00643
    • 00651
    • 00674
    • 00675
    • 00677
    • 00678
    • 00679
    • 00687
Amount recalled
430

Where it was sold

Why it was recalled

Software Version 02-26, when used with the Central Nursing Station (CNS) 6201, (PU-621 RA) may unexpectedly and without warning reboot, resulting in a period of approximately 3 minutes during which time the system does not display patient data and does not emit alarms based on that data should they be appropriate.

This product could cause temporary or reversible health problems — stop using it.

Want the full recall guide?

The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.

Free recall alerts

Get alerted about new Nihon Kohden America Inc. recalls

One email when a matching recall is published. No account, no cost, unsubscribe in one click.

Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Notice updated Apr 28, 2015 · Data as of Sep 19, 6:05 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.