See a list of details to help identify the product
Reason the product is recalled
Some units of the Total Knee device may contain faulty pins based in the axis of the knee.
The hazards to consumers
Illness or mistreatment (Class 2).
Details to help identify the product
Supplier running the recall
Ossur Asia-Pacific
Where the product was sold
Nationally
Responsible regulators
Regulators are established or appointed by government. They enforce regulations and rules.
Quote PRA number 2006/8487 when contacting a regulator about this recall.
Recall and remedy questions
Contact the Therapeutic Goods Administration if you have:
- a question about the remedy being offered to you by the business that is responsible for managing this recall, or
- concerns about the way the business is managing this recall.