DePuy Knee Replacement unit Recall

So far, there’s not been a recall of the Attune system, despite records of high rates of failing. In 2015, an element of the machine was recalled after DePuy discovered that a wire spring and coil coil in the Attune Leg Tibial Articulation Surface Devices was susceptible to damage.

The Category II Device Recall handled more than 3,000 products.

DePuy Knee Replacement unit Lawsuit Filed

Shortly after the discharge of the analysis citing loosening in the Attune system, a company submitted the first lawsuit against DePuy Synthes over statements that these devices prematurely failed.

The lawsuit was submitted in Sept 2017 in the Circuit Judge of Tuscaloosa Region by Cunningham Bounds LLC. The lawsuit alleges that Johnson & Johnson and its own subsidiary DePuy Synthes created a faulty device.


Knee replacement unit surgeries are done when someone has a broken joint that triggers significant pain and reduced freedom. You can also browse to know more about the depuy attune knee lawsuit.

If knee destruction, caused by joint disease, injury, or other notable causes, is bad enough, it can limit a person’s activity and critically hamper standard of living. Therefore, the potential risks of major surgery tend to be regarded as outweighed by the benefits associated with obtaining a new knee.

There will vary types of leg replacement surgery, depending on type and magnitude of harm to the joint. For a complete knee replacement, the complete joint is changed with an entire, working man-made joint.

When destruction is not in depth, a surgeon can do a partial leg replacement. This calls for removing ruined bone and cells and swapping it with the required man-made parts. When part of artificial leg fails, a doctor may execute a revision surgery.

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