RecallDepth

Multi Parameter Patient Monitor (with Arrhythmia Detection and Alarms) Product Usage: The V Series Monitor is intended for intra hospital use under the direct supervision of a licensed healthcare practitioner. The indications for use for the V Series include the monitoring of the following human physiological parameters: 1) ECG waveform derived from 3, 5, 6 and 12 lead measurements 2) Heart Rate 3) Pulse Oximtery 4) ST Segment 5) Arrhythmia Detection 6) Non Invasive Blood Pressure (IBP) 7) Cardiac Output (CO) 8) Respiratory Gases 9) Respiration Rate 10) Temperature The V series monitor has the capability of performing IV Drug and Hemodynamic Calculations and interfacing with network devices.

Company
Mindray Ds Usa, Inc. D.B.A. Mindray North America
Recall Initiated
October 7, 2013
Posted
November 25, 2013
Terminated
April 27, 2015
Recall Number
Z-0389-2014
Quantity
1839 units
Firm Location
Mahwah, NJ

Reason for Recall

Mindray has identified an issue with V Series Monitor where the V Dock power pins connecting the V Series Monitor to the V Dock may lose spring tension, potentially causing the screen to temporarily go blank, lose communication with the central station monitor (when one is in use) or shut down. No patient related events have been reported to Mindray concerning the issue.

Distribution

Worldwide Distribution - USA Nationwide

Lot / Code Info

V Series Montor p/n 0998-00-1801-01 and the associated V Dock , p/n 0998-UC-180-01

Root Cause

Environmental control

Action Taken

Mindray sent an Urgent Corrective Action letter dated October 7, 2013 to all of their customers. The letter identified the affected product, problem and actions to be taken. Customers should contact their Mindray Service Representative at 1-800-288-2121 Monday through Friday from 830 am to 530 pm to arrange for the replacement of the affected product.

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