Medical device recalls Moderate risk

Mindray DS USA, Inc. dba Mindray North America recalls Panorama Patient Monitoring Network Mindray DS USA The Panorama Patient Monitoring can view recal time, store, print, g…

Recall date
March 9, 2016
Source
U.S. Food & Drug Administration (FDA) — enforcement report
Recall number
Z-1575-2016
FDA classification
Class II
Brand / firm
Mindray DS USA, Inc. dba Mindray North America
Sold / distributed
Nationwide Distribution

Why it was recalled

Panorama Central Station including the work station View Station, View Station and the eGateway will revert to the year 2000 when Daylight Savings Time (DST) occurs on March 13, 2016, or under various conditions.

Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.

What was recalled

Panorama Patient Monitoring Network Mindray DS USA The Panorama Patient Monitoring can view recal time, store, print, graph and trend patient clinical and demographic data. The Panoram Patient Monitoring Network can sent independent alarm limits for data send by the bedside monitor.

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