Guidant Corporation voluntarily notified doctors on July 18 th 2005 of a potentially fatal in nine of their pacemaker models, including the Pulsar Max. The company also notified the United States Food and Drug Administration in order for the agency to determine this course of action as a recall. Guidant admitted that at least 69 of these models manufactured between 1997 and 2000 had failed causing 20 pacing failures, five incidents of fainting, and possibly one death.

A pacemaker is a small device implanted directly into the chest that provides constant electrical stimulation in order to maintain a steady heartbeat. Hearts that are damaged due to injury or disease are often the best candidates for pacemakers. Unfortunately, the hermetic seal that connects the halves of the device together is prone to failure in some models which allows moisture to corrupt the delicate electronics inside.

Warning signs of a malfunctioning pacemaker include:

• Early batter depletion
• Irregular heart pacing
• Inappropriate reset warnings
• Advanced replacement warnings

If you or someone you know has a Guidant Pulsar Max Pacemaker model numbers 1170, 1171, or 1270, contact a medical professional right away. Also let your doctor know if you use any of the following affected pacemakers:

Pulsar | Discovery | Discover II | Meridian | Virtus Plus II | Intelis II | Contak TR | Pulsar Max II

Once you have ensured your safety, contact an attorney. You may be entitled to reparations based on your individual case. Take a stand against irresponsible corporations who put their profits ahead of your wellbeing.

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