If you received the DePuy CMF Distraction System and believe you suffered injuries as a result, contact Attorney Group for Arkansas today for information about your legal options or about pursuing a claim for compensation. In a free, no obligation consultation, we can determine whether you are eligible to file a lawsuit. If you are, Attorney Group for Arkansas can connect you with an affiliated attorney. He or she can file a lawsuit on your behalf and help you seek damages for your condition.
DePuy CMF Distraction System Recalled
The DePuy Craniomaxillofacial Distraction System was designed to lengthen and stabilize the lower jaw and jawbone following birth defects or post-traumatic injuries. According to the manufacturer, both adults and children, including babies, can receive the device. However, DePuy received 15 reports from patients who experienced injuries allegedly resulting from the device.
DePuy contacted hospitals on April 26, 2014, and requested that the hospitals remove the product from their inventory. Four months later, the U.S. Food and Drug Administration (FDA) issued a Class I recall to remove the product from the market. A Class I recall designation means that use of the product may cause severe injury or death.
According to the recall notice, the DePuy CMF Distraction System may reverse direction and lose its intended distraction distance following surgery. Infant patients may suffer from sudden tracheal obstruction, which can lead to respiratory arrest and death. In older patients, failure may require surgical intervention to remove and/or replace the device.
Is the DePuy CMF Distraction System Safe?
Individuals who may be at the highest risk of injury include infants or young children. While adults and older children may still be able to breathe should the device fail, babies and children who do not yet have complete control over their airways may become injured or die.
According to several patients allegedly harmed by the device, removal procedures were necessary in order to correct the damage caused by the device. As a result, patients may consider working with an attorney to learn more about their legal options and pursuing a claim for compensation in an Arkansas DePuy Jaw Implant Lawsuit. Family members who lost family members due to respiratory arrest, tracheal obstruction, or other fatal complications may be eligible to file a wrongful death lawsuit on behalf of their loved.
Importance of Legal Counsel
The unexpected and added expense of medical procedures, medications, treatments, and other costs associated with device failure can prove to be a serious problem for many patients. As a result, individuals wishing to seek compensation for these and other damages should consider working with a defective medical device attorney in Arkansas. Although compensation is never guaranteed, you may be eligible to receive compensation for pain and suffering, lost wages, or a loss of earning capacity.
Contact Attorney Group for Arkansas Today
If you were fitted with the DePuy CMF Distraction System and suffered injuries you believe were caused by the device, contact Attorney Group for Arkansas today. In a free, no obligation consultation, we can determine whether you are eligible to file a lawsuit. If you are, Attorney Group for Arkansas can connect you with an affiliated Arkansas attorney. He or she can file a lawsuit on your behalf and assist you throughout the legal process. Call today.
