Reported Mar 19, 2014 · Terminated

Panaroma Central Station Product Usage: This device can view real time, store, print, graph, and trend patient clinical…

Mindray DS USA, Inc. dba Mindray North America

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: Mindray DS USA, Inc. dba Mindray North America · 800 MacArthur Blvd · Mahwah, NJ · 07430-2001

Is this the product you have?

  • Panaroma Central Station Product UsageThis device can view real time, store, print, graph, and trend patient clinical and demographic data. The device can also set independent alarm limits for data send by the bedside monitor
Lot codes and dates
    • p/n 0998-00-0708-01
    • 0998-UC-0708-01 and 0020-00-0205-XXX
Amount recalled
732 units in the US

Where it was sold

  • Nationwide

Why it was recalled

Mindray has identified two issues with the Panorama Central Station. Full Disclosure data may lag behind the Panorama system time clock when the Panorama Central Station is in use with Mindray¿s V-Series Monitor. Additionally, event indicators lag behind the Panorama system time clock when the Panorama Central Station is in use with a Panorama Telepack.

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

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Where this came from

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

Read the FDA (openFDA device enforcement) notice

Notice updated Jan 21, 2015 · Data as of Sep 19, 4:49 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.