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Guidant Pacemaker Recall Lawyer - Guidant Lawyers - Guidant Defibrillator Recall Lawyer
Indianapolis-based Guidant has recalled 136,950 Guidant Defibrillators and Pacemakers. The company said about 63,000 of the devices had been implanted, with nearly 50,000 still in use. Guidant stated that the devices could, without warning, develop a short circuit that would prevent them from delivering the shock when needed. There have been reports of at least 45 malfunctions and are thought to have caused several deaths. Find a Guidant Pacemaker and Defibrillator Lawyer in your state.
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Hip Replacement Recall
Have you had a hip replacement? If so, the components used to replace your hip may be defective. On August 26, 2010, DePuy Orthopaedics, Inc., a division of Johnson & Johnson, announced a worldwide recall of two separate hip replacement systems.
Hipreplacementrecalllawsuit.org ~
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