The Cochran Firm Legal Blog

More than 14,000 external defibrillators have been recalled due to product defects resulting in 39 injuries, two of which were fatal. The models included in the recall are AED 10 and MRL JumpStart defibrillators.

Defects in these defibrillators have led to low-energy shocks in patients, electromagnetic noise interference, and sudden shutdown of the device. These defects have prevented patients from receiving necessary treatment in the event of cardiac arrest.

The recall was initiated by Welch Allyn, the company that manufactures the defibrillators. The company is advising patients to continue using these devices until they receive replacements, since the likelihood of a malfunction is minimal.

If you are currently, using an AED 10 or MRL JumpStart external defibrillator for your heart condition, consult your doctor immediately to find out the proper protocol for replacing the device. If you have suffered an injury from one of these devices, you should report the incident to the Food and Drug Administration (FDA) as soon as possible.

The experienced product liability attorneys at The Cochran Firm can help you receive the compensation you deserve if you have suffered an injury from using a defective medical device.

Please contact one of our defective product lawyers today to schedule a consultation. We serve clients nationwide.