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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