Zimmer Biomet is conducting a medical device recall for one (1) lot of the Dual Mobility Vivacit-E® bearing due to a commingle. The outer package is labeled as a size G 46 mm, however, the implant inside the package is a size F 44 mm. One (1) complaint has been received that identified the size discrepancy at the point of use during the procedure. The defectiveness was discovered on September 19, 2025. Issue was identified through the complaints handling process.
RecallTracker