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Recall for the ISKD, ORTHOFIX
2012.08.31
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