Thoratec Corporation has warned that their HeartMate II blood pump may fail due to a defective lead that connects the heart pump with the System Controller. The lead has been found to wear or fatigue over time, potentially interrupting pump function. At least 27 people have required surgery to replace the mechanical heart, and five deaths have been linked to the HeartMate lead problems. Continued
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Thoratec HeartMate II Artificial Heart Lawsuits
On October 15, 2008, Thoratec Corporation issued a warning for the HeartMate II Left Ventricular Assist System after it was discovered that the percutaneous lead connecting the blood pump with the System Controller could wear or fatigue, potentially causing interruption of pump function. Continued
