guidant pacemaker

Guidant was a spinoff of Eli Lilly Co which separated the company to focus on pharmaceutical drugs. Guidant Corporation, which has a $25.4 billion acquisition offer pending from New Brunswick, N.J.-based Johnson & Johnson. According to a letter from Guidant to the medical community, Guidant’s Cardiac Rhythm Management Quality System determined that a hermetic sealing component utilized in these devices may experience a gradual degradation, resulting in a higher than normal moisture content within the pacemaker case late in the device’s service life. This decision will depend on many factors, including the patient’s condition and medical history. Pacemakers are considered a contraindication for commercial and military diving. Do not stop taking a prescribed medication without first consulting with your doctor. Although the risk of failure in the devices is low, the risk is significant enough to advise patients that have had the recalled devices to seek the advice and opinion of a doctor. Guidant Pacemakers send electrical pulses to the heart to accelerate a slow heart beat, and have a seven- to 10-year life span before they must be replaced. Currently, Guidant faces over 100 individual and class action lawsuits related to its defibrillator and pacemaker products. According to Guidant, loss of pacing output had been found in 36 Insignia and Nexus pacemaker devices out of 49,500 that had been distributed worldwide. It has been reported by Guidant, that device failures in these lines have not lead to any known deaths but the device failures are linked to nine emergency hospitalizations. Premature battery depletion resulting in loss of telemetry and/or loss of pacing output without warning; Inappropriate accelerometer function (if programmed ON), resulting in sustained pacing at the programmed maximum sensor rate (MSR); Lack of appropriate accelerometer rate response during activity; Appearance of a reset warning message upon interrogation; and. Issues such as these led to at least nine hospitalizations and for Guidant to recall a significant number of the devices. Guidant stated that the devices could, without warning, develop a short circuit that would prevent them from delivering the shock when needed. Some pacemakers may include a defibrillator to automatically restart the heart during heart failure. Pacemakers : Meridian: SSI: 476: Produced 11/25/97 - 10/26/00 -- Problem: Prolonged tachycardia, syncope, dizziness or heart failure -- Solution: Reprogram : SSIR: 1176: Produced 11/25/97 - 10/26/00 -- Problem: Prolonged tachycardia, syncope, dizziness or heart failure -- Solution: Reprogram : DDD: 976 Instead of halting production and recalling the units, Guidant decided to continue to sell faulty devices and address the malfunction in later models. Guidant however, continued to manufacture the devices and users were not told of the failure reports. Guidant was a spinoff of Eli Lilly Co which separated the company to focus on pharmaceutical drugs. Everyday throughout the world a person injured or killed as a result of a helicopter crash or aviation accident. Common signs of pacemaker failure include shortness of breath, dizziness, lightheadedness or a prolonged fast heart rate.

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