BfArM - Federal Institute for Drugs and Medical Devices

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Product group Dental products
Reference 01672/08

The company BIOMET UK Ltd. informed about a recall respectively a field corrective action concerning the product Stella Osteotome (catalogue numbers 01-575, 01-576, 01-578). It has been identified that the working tips were thicker than specification. Possibly that leads to a damage of surrounding anatomical structures while performing an interdental osteotomy.

Recall Stella Osteotome, BIOMET , Download_VeroeffentlichtAm_EN PDF, 107KB, File does not meet accessibility standards