Mindray DS USA, Inc. d.b.a. Mindray North America

9 recalls Categories: Other Medical Devices, Diagnostic Equipment, Infusion Pumps

Mindray has identified a software anomaly that may where, in the presence of an asystole, the Telepack ECG waveform may produce a unique step pattern (instead of a flat line) if Lead 1 or V is being utilized for detecting cardiac arrhythmia.

Nov 28, 2012 Diagnostic Equipment Nationwide View Details →

There is a software anomaly with the DPM Central Monitoring System where the trend data of one patient maybe replaced with the trend data of a second patient.

May 12, 2011 Diagnostic Equipment Nationwide View Details →

Mindray has identified an issue with the V Series Monitor where the monitors touch screen may stop responding to touch.

Sep 24, 2012 Diagnostic Equipment Nationwide View Details →

There is an issue with the DPM 6 and DPM 7 monitors where the following features may be unavailable : Full Disclosure, Drug, Hemodynamic Calculations, Renal Calculations, Oxygenation Calculations, and Ventilation Calculations.

Aug 11, 2010 Diagnostic Equipment Nationwide View Details →

Mindray has identified the potential for a system leak resulting an issue related to the carbon dioxide absorber canister gasket on A3/A5 Anesthesia Delivery Systems. A potential system leak resulting from the canister gasket will likely present itself during the Automatic Circuit Leak and Compliance Test performed at startup and the Manual Leak Test recommended to be performed before each case.

Aug 13, 2012 Infusion Pumps Nationwide View Details →

Mindray has identified the potential for a system leak resulting an issue related to the carbon dioxide absorber canister gasket on A3/A5 Anesthesia Delivery Systems. A potential system leak resulting from the canister gasket will likely present itself during the Automatic Circuit Leak and Compliance Test performed at startup and the Manual Leak Test recommended to be performed before each case.

Aug 13, 2012 Infusion Pumps Nationwide View Details →

Mindray has identified two software anomalies contained in the V Series Monitoring System. There have been no reports of injuries associated with these anomalies. These anomalies affect V Series Systems distributed between September 31, 2010 and January 9, 2012.

May 7, 2012 Diagnostic Equipment Nationwide View Details →