Archive for April, 2010

There are lots of different types of defibrillators. An automated external defibrillator (AED) is a portable electronic device that diagnoses and treats cardiac arrest by re-establishing an effective heart rhythm. This treatment is called defibrillation, which applies an electric shock to the whole heart muscle, uniformly clearing the electrical activity of the heart and makes it possible to synchronize hopefully.
An AED is called external because the operator applies the electrode on the bare chest of the victim, unlike internal defibrillators, the electrodes were surgically implanted into the body of a patient. There are two main types of AEDs on the market today: semi-automatic and fully automatic.
Semi-automatic AEDs prompt the user was clear and then push a shock button to defibrillate. Fully automatic units sound booth clear message and then deliver the shock automatically without the user pressing a button.
AEDs in corporate and government offices, shopping centers, airports, restaurants, hotels, sports stadiums, schools and universities, cultural centers can be found, and other places to gather in large groups of people and the risk of sudden cardiac arrest incident is likely. In some cities, all police vehicles carry an AED. All hospitals, fire and medical personnel to use AEDs to heart problems and address. These AEDs are a critical tool for emergency medical personnel who use them. It is therefore extremely important that these devices reliable, but often the difference between life and death for thousands of people each year.
Access Cardio Systems, Inc. Emergency Defibrillator Failures
In the year 2005 gives the Food and Drug Administration (FDA) a global recall of Access Cardio Systems, Inc. Emergency defibrillators were found as they avoid defective components of the device could to ensure a proper shock. It was noted that two problems may occur in these defibrillators. Some of these defibrillators have a catastrophic failure of the shock delivery circuit board that prevents the delivery of additional shocks. Others were found to turn up unexpectedly, so the “on / off” switch to no effect, and the batteries are exhausted. After such a failure of the device is not working properly or not defibrillation. Because the Access recalls Cardio Systems, Inc., the manufacturer of defibrillators, went out of business. It is not possible, all available parts for each of the machines that were not found to replace it as defective. The FDA has recalled many of these defibrillators, and has advised all Access Cardio Systems, Inc. customer immediately the use of equipment and devices, to find substitutes elsewhere.
The FDA points out, Access Cardio Systems, Inc. Emergency Defibrillators
As part of FDA oversight of medical devices, the department has developed a classification system that remembers three classes, the class includes I, II and III. Class I recalls, the most serious type of memory, and shows that there is a realistic chance that the product of serious health problems or death. The FDA has issued a Class I recall of the following Access Cardio Systems, Inc. Device:
. AccessAED PAD (without ECG) Public Access Defibrillator (Model # 9100-0010-0)
. AccessAED PAD package (without ECG) (Model # 9100-0015-0)
. AccessAED Package (without audio recording) (Model # 9100-0150-0)
. AccessAED (without audio recording) (Model # 9100-0100-0)
. AccessAED (audio recording) (Model # 9100-0100-1)
. AccessALS (Advanced Life Support) (Model # 9100-0100-2)
. AccessAED package (audio recording) (Model # 9100-0150-1)
. AccessALS Package (Model # 9100-0150-2). In Class II recall, there is a possibility that the medical device will cause temporary or reversible health problems, or there is a remote chance that the device can lead to serious health problems.
The FDA granted the following Class II recalls the Access AED and Access ALS Automated External Defibrillators (Model # 9100-0100). should have experienced people, health problems or injuries associated with these devices can be legal advice, as they may get in a position to benefit financially. At that time, the company offers not just any refunds for those organizations that bought the faulty devices.