BfArM - Federal Institute for Drugs and Medical Devices

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Product group Non-active implants
Reference 03068/08

ΩConnector: The company HEINZ KURZ has informed about a lot recall of these products. The action was initiated because of a failure in ball diameter, so that the ΩConnector possibly cannot be fitted well into the KURZ middle ear total prosthesis.

Recall for ΩConnector, HEINZ KURZ , Download_VeroeffentlichtAm_EN PDF, 30KB, File does not meet accessibility standards