BfArM - Federal Institute for Drugs and Medical Devices

Navigation and service

Product group Non-active implants - bone surgery
Reference 05375/12

Intramedullary skeletal kinetic distractor, ISKD: The company ORTHOFIX has informed about the recall of these products. The action was initiated because of the possibility of a post-operative malfunction (stop distracting during treatment).

Recall for the ISKD, ORTHOFIX , Download_VeroeffentlichtAm_EN PDF, 215KB, File does not meet accessibility standards