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┬áComprehensive Reverse Shoulder Humeral Tray (Model 115339) following reports that the devices are fracturing at a higher rate than stated in the labeling. In December Zimmer Biomet had sent an Urgent… Read More


Biomet, Inc. and counsel for Plaintiffs reached an agreement to settle all cases currently pending in the Biomet MDL (In Re Biomet M2A Magnum Hip Implant Products Liability Litigation, MDL 2391) and any future cases filed on or before April 15, 2014. To be eligible for compensation a plaintiff must have been implanted with a Biomet M2a 38 or M2A Magnum hip replacement system and underwent surgery to revise the device more than 180 days after it was implanted.… Read More