Heart Sync Inc. issues Device Correction-Pad Connectors for Defibrillator Units

Today the FDA announced another product correction.  Heart Sync, Inc issued a voluntary correction due to a connector compatibility issue with Philips FR3 and FRx Defibrillator Units.

The electrodes in the product correction with not connect to the Phillips Fr3 and FRx units.  This may not be discovered until the AED unit is used.  This may result in a delay in delivering the electrical therapy and could lead to death or other serious consequences.

Click to read the full FDA notice here.

If you or a loved one have been injured by a defective medical product, please contact the attorneys at the Ruth Law Team, 1-888-783-8378.