BfArM - Federal Institute for Drugs and Medical Devices

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Product group Non-active implants - bone surgery
Reference 00844/12

ChronOS Putty: The company MATHYS has informed about the recall of products. The action was initiated because of a fault in the Instruction For Use. There is a misleading description on how to open the sterile packaging which may cause non-sterility.

Recall for chronOS Putty, MATHYS , Download_VeroeffentlichtAm_EN PDF, 358KB, File does not meet accessibility standards