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LAWSUITS NEWS & LEGAL INFORMATION

Stryker ShapeMatch Lawsuit Survives Motion to Dismiss

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Lafayette, LAA Stryker ShapeMatch lawsuit has survived a motion to dismiss by the defendants, although the plaintiff has been told she must amend her complaint. The ShapeMatch Cutting Guide lawsuit alleged the plaintiff was harmed by the use of the cutting guide, which was recalled since her surgery.

According to court documents, Ouita Corley had knee replacement surgery on March 30, 2009, and her surgery involved the use of the Stryker ShapeMatch Cutting Guide.

The ShapeMatch Cutting Guide, manufactured by Stryker Orthopaedics, is a single-use cutting guide, designed to help surgeons with knee replacement surgeries. Specifically, they were meant to be used along with an MRI to create an image of the patient’s knee to show the surgeon where to make incisions in the bone for implantation of knee components. The ShapeMatch Guides were supposed to allow surgeons to make smaller incisions in the patient’s knee and customize the surgery to each individual patient.

In April 2013, Stryker issued a Class I Medical Device Recall of the ShapeMatch. The recall was initiated after the FDA received 44 reports of events - including malfunctions - of the ShapeMatch Cutting Guide.

In August 2013, Ouita Corley filed a lawsuit against Stryker, alleging that her knee was misaligned due to the defective nature of the ShapeMatch. As a result, Corley reportedly suffers significant pain, discomfort, joint instability and limited mobility. Her lawsuit claims that diagnostic testing showed her knee is misaligned and must be replaced. Replacing the implanted knee device will require additional hospital time and hospital expenses.

Stryker filed a motion to dismiss the lawsuit, arguing that Corley’s complaint did not allege sufficient facts under the Louisiana Products Liability Act. Although the judge agreed with Stryker that the plaintiff’s lawsuit did not meet the requirements of the Louisiana Products Liability Act, he found that Corley should be given the opportunity to amend her complaint. As a result, he denied the motion to dismiss the lawsuit and gave Corley 30 days to file an amended complaint. Should she fail to do so, the defendants could again file a motion to dismiss.

The lawsuit is Corley v. Stryker Corporation, number 6:13-cv-02571, US District Court, Western District of Lousiana.

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READER COMMENTS

Posted by

on
Surgery 10/22/12 has been painful since although was able to achieve PT motion flex goals.. Operating Orthopedic kept saying it was me, he found nothing wrong and ultimately strung me along to 2 yrs before he cut me off pain meds and said I would have to see a Neurologist for pain management. So been chasing my tail since then to get relief but only getting worst same symptoms as Moses above. Now desperate to find Class Action Suit to join or learn what solutions those sharing the same problem are using. Invite dialog with any and all on this problem, am off pain patch and Vicodin so biting the bullet to endure and it is really affecting my quality of life. Please share your experience..

Posted by

on
Had a Stryker Triathlon total knee replacement August 19th 2014. In November my knee started popping out of place or 'Hydroplanning' as the doctor would describe and causing chronic pain. I informed my doctor and PT of this and was told it was normal untill my muscles stabilize. It is now December 15th 2015 and the popping has gotten worse, with loud clickes and grinds with any movement Of my leg. I cannot bend my knee back without pain, I cannot stand or walk without a cane and sometimes walker. I have no feeling on the outer portion of my leg down to my shin...unless someone or something presses up against it and it causes great pain. I have not been able to substan any employement, do to the fact that I cannot stand long without my knee going numb and I can only walk short distance because my knee is constantly in pain. I cannot drive because my knee pops out of place I have to rotate position of leg just to try and find relieve as well as being in fear of having an accident. My doctor has been informed of these symptoms.

Posted by

on
The stryker salesman failed to report adverse events at orthopedic institute of souh Florida doctors hospital. When he was in the surgery

Posted by

on
I had both knees replaced with Stryker Triathlon parts. One in 12/912 and the other in 1/13. Both knees are unstable @ less than 2 years after surgery. I have now had to have one of them replaced in a Revision Surgery and the other will need to be done in the future. The new OS will probably never testify to it but he told me that they were not balanced correctly.

Posted by

on
left knee
Pain, swelling, clicking,the outside of my knee is totally numb does not have motion as right knee. I cannot put any pressure on my left knee, if I was to get on knees, would be impossible to get up. I know that I need to have stryker knee replaced, but dread going thru operation at this time. when out , I need someone with me to keep balance.
I was never notified by my DR. of recall. I have my surgical reports and list of parts from stryker that was used.

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