FDA Recalls Zimmer Biomet Shoulder: High Fracture Rate
By Marilyn T. McGoldrick, Esq. Published on April 13, 2017 Class 1 Recall The FDA has announced a Class 1 Recall of the Zimmer Biomet Comprehensive Reverse Shoulder Humeral Tray (Model 115339) following reports that the devices are fracturing at a higher rate...
Fluoroquinolones Linked to Aortic Dissection and Aneurysms
Call 888-341-1405 for a free consultation with a recognized leader in defective drug and personal injury litigation. You can also contact us online to tell us your story. By: Marilyn McGoldrick, Esq. Published on March 20, 2017 Aortic aneurysms and dissections have...
FDA Backs Xarelto Despite Flawed Clinical Trial
Thornton Law Firm is no longer accepting new Xarelto cases. By: Marilyn McGoldrick, Esq. Published on February 1, 2017 Recently, issues were raised concerning the results of a clinical trial for the blood thinning drug Xarelto. It was discovered that a medical device...
FDA Approves New Morcellator Device Despite Cancer Concerns
Call 888-341-1405 for a free consultation with a recognized leader in personal injury and medical device litigation. You can also contact us online to discuss the details of your case. By: Marilyn McGoldrick, Esq. Published January 17, 2017 In 2014, the U.S. Food...
