medical Class II Updated 2021-10-06

Corin Ltd recalls Corin Unity Knee Augments, Size 5, 6 & 7 / 10mm Thick, Femor

Recalled Product

Corin Unity Knee Augments, Size 5, 6 & 7 / 10mm Thick, Femoral Posterior Augment, REF 1122370, Sterile, a component of the Unity Total Knee System.

Hazard / Issue

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.

Issued by

FDA

Distribution: Nationwide (United States)
Lot/Code Info: The affected products are shipment specific and were delivered to the consignee between 7/22-26/2021. Lot number 472687 was delivered 7/23/2021.
View official government recall

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