Philips AED Recall in 2018 – Defibrillator Failure May Have Harmed Hundreds

Defective Devices

Defibrillators are vital when it comes to the prevention of cardiac events if, when not treated in a timely manner, may lead to a full-on heart attack. These are portable devices which discharge electrical current in order to restart the heart or correct arrhythmia, and must be manufactured in a sound manner because any room for error may cause severe injuries or death to the patient. Late last year, the FDA issued a Philips defibrillator recall when it was discovered that these machines have a manufacturing defect which would cause gas to leak from inside the device, causing a malfunction that is not easy to detect.

Were you or a loved one hurt by the Philips AED defibrillator? If you suffered extensive injuries such as burns, of if a loved one died due to a malfunctioning defibrillator which failed to provide a much-needed electrical shock, you may be able to file a Philips defibrillator recall lawsuit. Simply pick up the phone and give us a call NOW at 1 (773) 825-3547 to speak with our friendly and experienced attorneys. We’ll help you discover the next steps to take to file your claim as well as give you a ballpark amount of what your case is worth in relation with your injuries so you can recover compensation in as little time as possible.

FDA Philips AED Recall – Get the Details Here

The FDA, in conjunction with Phillips, issued a recall notice last year for various models of the HeartStart MRx Defibrillator when it was discovered that there was a defect in the Gas Discharge Tube, or GDT. The findings showed that the tube has tiny cracks which inadvertently cause gases to be released out of the device, leading to defibrillator malfunction. In addition, this gas leakage issue causes an electrical charge surge which may cause damage to its resistors, thereby leading to the failure of the device when in AED mode.

The FDA directive also said that the HeartStart MRx will work as expected when placed in manual mode. However, the EKG display will be hard to read or interpret due to device noise. Devices affected are those manufactured between September 22nd 2016 and October 31st, 2016, and those that have M3535A as well as M3536A item/model numbers.

Philips AED Recall Is Just The Tip of The Iceberg

The FDA, in communication in previous years, mentioned that defibrillators from various manufacturers have been plagued by numerous problems due to egregious and unacceptable errors in manufacturing as well as designing, and the failure to enforce industry practices by the makers of these devices. The government agency also added that many of these companies have handled customer complaints poorly, and haven’t conducted defibrillator recalls in a timely manner, which may have cost some people their lives.

Philips MRX Defibrillator Lawsuit – We Can Help!

It is important to note that the Philips AED recall 2018 event will not precede a class action lawsuit. Cases like this may be collated into multidistrict litigation which will help them move faster, as well as afford individuals affected a much higher payout. If you have been injured by the Philips defibrillator and are curious about the payout as well as what you can sue for, please give us a call at 1 (773) 825-3547 and speak with an experienced and friendly attorney for free to learn more about your legal options. Thanks, and we look forward to hearing from you.