BfArM - Federal Institute for Drugs and Medical Devices

Navigation and service

Instructions for Use Recall "Navigation Pin, Ortholock EX Pin and Ortholock", Stryker

Product group Surgical equipment/ Anaesthesia
Reference 02393/08

The company Stryker Leibinger GmbH is conducting a recall of the Instruction for Use for Stryker Navigation Pin, Ortholock EX pin and Ortholock. The instructions have been updated to include warnings regarding aspects of percutaneous pin placement during navigated knee surgery in order to prevent femural stress fractures. Users received a letter with summarized warnings.

Instructions for Use Recall "Navigation Pin, Ortholock EX Pin and Ortholock", Stryker , Download_VeroeffentlichtAm_EN PDF, 101KB, File does not meet accessibility standards