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Recall Observatory FDA recall evidence

Device product

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.

Z-0389-2014

October 07, 2013

Class II

Product summary

Firm
Mindray DS USA, Inc. dba Mindray North America
Event
Event 66755
Status
Terminated
Classification
Class II
Quantity
1839 units
Official record key
device-enforcement:Z-0389-2014

Official wording

Reason: 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.

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

Distribution pattern: Worldwide Distribution - USA Nationwide

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

    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.