BfArM - Federal Institute for Drugs and Medical Devices

Navigation and service

Product group Optics / Precision engineering
Reference 00205/08

Recall of the Stryker burs for use with “R” and RX” attachments (all lots and article numbers see annex). The reason for the recall is potential packaging material degradation of the a.m. products caused by UV exposure etc. The risk is a constricted sterility of the products.

Recall burs, Stryker , Download_VeroeffentlichtAm_EN PDF, 93KB, File does not meet accessibility standards