Medtronic Recall
On January 22^(nd), 2018 there was a Class I recall by the Food & Drug Administration (FDA) for Medtronic’s Cardiac Resynchronization Therapy (CRT-D) and Implantable Cardioverter Defibrillator (ICD). It should be noted that Class I recalls are a rare thing and that when a Class I recall does happen the FDA implements a specialized strategy to best combat the situation.
The goal here is to remove the product from all commercial stores and to ensure that all who are using the product are safe. This includes removing the product from people’s possession completely or replacing it with a non-defective model. These are important facts to consider if you or someone you know has one of these Medtronic products, they should be informed immediately if they haven’t already.
While there is an admitted error with the product being recalled, receiving compensation is not always as easy as you might think. If you or a loved one are affected by the 2018 Medtronic recall it is important that you contact our Medtronic recall attorneys at Webster Vicknair MacLeod today. We can guide you through the process in an attempt to receive the compensation you deserve.
