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Type of Product	Medical Device
TGA Recall Reference	RC-2012-RN-01003-1
Product Name/Description	Triathlon CR/PS Inserts & ASYM Patella, Brunswik Captive Cemented Cup, Avon Patella Medium & Patella Femoral Joint, HMRS Humerus Bearing, MRH Bumper Neutral/3 Degrees & Tibial Inserts, Scorpio CR Tibial Insert & Medialised Patella, Duracon PCA Femoral, Patella & Constrain Inserts, Scorpio PS Tibial & Flex PS/+PS/+PCS Inserts (total knee, hip, shoulder components) and Artisan Bone Plug Multiple item and lot numbers ARTG:128028, 139146, 128021, 128026, 139145, 145124, 128448, 141151 & 142278
Recall Action Level	Hospital
Recall Action Classification	Class II
Recall Action Commencement Date	4/10/2012
Responsible Entity	Stryker Australia Pty Ltd
Reason/Issue	Stryker Orthopaedics has become aware of a potential packaging issue associated with various products, potentially affecting sterility of the devices.
Recall Action	Recall
Recall Action Instructions	Quarantine the affected devices identified in customer letter from Stryker.
Contact Information	1800 803 601 - Stryker Regulatory Affairs