Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Corin Unity Knee Augments Recalled by Corin Ltd Due to The packaging system on the devices have potential...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Corin Ltd directly.
Affected Products
Corin Unity Knee Augments, Size 5, 6 & 7 / 10mm Thick, Femoral Posterior Augment, REF 1122370, Sterile, a component of the Unity Total Knee System.
Quantity: 1 unit
Why Was This Recalled?
The packaging system on the devices have potential physical and water damage resulting in damage to the devices, loss of sterility, or contamination of the devices.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Corin Ltd
Corin Ltd has 21 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report