For years, patients and surgeons reported that the Cartiva implant was failing at alarming rates. Yet, the device remained on the market. That changed in October 2024, when a Class II Device Recall was finally initiated for the Cartiva Synthetic Cartilage Implant.

What the Recall Says: The recall notice acknowledges what victims have known for years: the device has a "higher-than-expected occurrence rate" of failure.

• Recall Date: October 31, 2024
• Recall Class: Class II (Situation where use may cause temporary or medically reversible adverse health consequences)
• Reason: High rates of revision, removal, implant subsidence (sinking), displacement, and pain.

Why This Matters for Your Case: A recall is a critical piece of evidence. It suggests that the manufacturer acknowledges the product is not performing as represented. If you received a Cartiva implant, your device is part of this recall.  Contact us today to discuss your options.