Mindray DS USA, Inc. dba Mindray North America: Medical Device Recalls in 2013

Updated on March 25, 2026.

According to to data from the FDA, there was 1 medical device recall made by Mindray DS USA, Inc. dba Mindray North America in 2013. See the detail of the recall below.

You can see similar recalls for other firms.

Data Source: FDA.

See this for other years:

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.