FDA warns Zimmer over adulterated devices at Puerto Rico plant The FDA told Zimmer in a warning letter that the company's Acetabular Cup products and the Trilogy Spike Cup products are being adulterated at its manufacturing facility in Puerto Rico. Reference Link
EU set to conditionally approve Zimmer, Biomet deal, Reuters reports The European Union is set to give conditional approval to Zimmer's proposed acquisition of Biomet, Reuters reports, citing two people with knowledge of the matter. Reference Link
Zimmer announces first clinical use of Vivacit-E liner Zimmer announced its first reverse shoulder replacement in the United States using Vivacit-E Liner for the Trabecular Metal Reverse Shoulder System.