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<h1>Exactech Knee And Hip System Recall Legal Professionals</h1>
The Exactech hip implant recall attorneys at our firm have a substantial quantity of expertise fighting for these who’ve sustained damage from their orthopedic medical devices. If you’re suffering from a debilitating and expensive implant failure, our compassionate group of consultants will work tirelessly to secure the compensation you have to transfer forward. Total hip replacements involve the implantation of both a femoral and an acetabular part. The acetabular liner, usually manufactured from some type of plastic, is inserted into an acetabular cup or shell that's positioned in the patient’s hip socket. The acetabular liner is positioned between the acetabular cup and a suitable femoral head. The Connexion GXL acetabular liner is manufactured from an ultra-high molecular weight polyethylene plastic, and based on Exactech, their acetabular liner manufacturing process results in less floor put on.

If you are experiencing any of these conditions or symptoms, seek medical attention immediately, and get in touch with an legal professional who can further advise you on your subsequent steps. I am very grateful to Sabrina Thornburg and Andrew Felix for every thing that they've carried out on my case. Sabrina kept in contact with me to let me know the way every little thing was going and I am very pleased with the service that she and Andrew supplied. If your surgeon contacted you about an Exactech recalled system, please get in touch with us to debate a possible declare against the product manufacturer. The product may be recalled as a specific lot is identified as being non-compliant and faulty. A product may be defective in manufacture or construction, supplies and assembly, and a manufacturer or distributor may be subject to strict liability, although it exercised all potential care.

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Patients who aren't suffering the aforementioned signs ought to talk about the recall with their physician on the subsequent regularly scheduled implant checkups. An x-ray of the implant should be taken and reviewed by your doctor, even if there aren't any symptoms of a failing implant. The material and data on these pages is intended to provide general data and not authorized recommendation.

Although Foxwell’s Optetrak implants functioned correctly at first, after a couple of years they began to fail. Foxwell began to experience significant swelling in his knees and legs and eventually skilled significant stiffness and grinding in his knee joints. In November 2021, Foxwell had to undergo revision surgery at which point it was discovered that his Exactech implant had failed. Patients who experience this failure experience pain and ultimately need to bear corrective revision surgery. The faulty packaging seems to have resulted in a significantly higher revision surgery rate. But oxidation causes the part components of the Optetrak, Truliant, and Vantage to considerably degrade over time.

Defective medical gadget litigation helps to enhance affected person security and holds medical gadget companies accountable when faulty merchandise injure plaintiffs and purchasers. Around 22 p.c have been beginning to endure from tibial implant loosening at only 25 months. Over a dozen of the reviewed sufferers wanted revision surgical procedure for tibial loosening, instability or pain.

Patients who obtained a recalled Exactech implant or replacement and subsequently suffered accidents associated to polyethylene degradation could qualify for a lawsuit. TRULIANT® – The TRULIANT® sequence of knee replacements are designed specifically for orthopedic surgeons places of work who want to streamline their implant surgical processes. These highly advanced knee replacements have been introduced in 2017 that are available three major variations to fit various totally different patient conditions and desires.


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