A pacemaker is a battery-operated device that helps the heart beat in a regular rhythm. They can be permanent (internal) or temporary (external). In America, an estimated 2.5 million people are living thanks to pacemakers. When the pacemaker is defective, heart rhythm problems may occur, causing the heartbeat to be too fast, too slow or irregular.
On July 18th 2005, the manufacturer of pacemakers, Guidant Corp., issued a worldwide warning for patients who had these devices implanted. They reported that nine defective pacemaker models from the ones manufactured between November 25, 1997 and October 26, 2000 are potentially defective. The brand names of such pacemakers are: Pulsar, Pulsar Max, Discovery, Meridian, Pulsar Max II, Discovery II, Virtus Plus II, Intelis II, and Contak TR. Reports from the defective pacemakers confirm loss of consciousness, and heart failures. Guidant Corp, indicated that one patient may have died because of the defective pacemaker. Specialists in the area warned the patients using pacemakers to replace it as soon as possible due to possible malfunctions or short-circuit.
After uncovering the information, Guidant Corp. has received 69 reports of failures. More than 28,000 patients got one of these devices implanted between 1997 and 2000. On September 22, 2005, Guidant had a recall for some of its Insignia and Nexus implantable pacemakers because of malfunction; in some cases emergency hospitalization was required. Some of the symptoms are shortness of breath, dizziness, lightheadedness or a prolonged fast heart rate.
Remember that if you or someone you know has a defective Guidant Pacemaker implant, you can be part of a possible class action lawsuit. You can qualify for damages or remedies, always longing to get the fair and right compensation. The one you deserve.