Hip Replacement Lawsuit Lawyers

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Stryker Hip Lawyers Nebraska - Toll Free 1-866-777-2557

Stryker Hip Lawyer Nebraska - Stryker Hip Replacement Lawyer Nebraska


If you or a loved one had hip replacement surgery and are experiencing certain side effects like metal poisoning or the need for a second revision surgery, you may be entitled to financial compensation from the manufacturer. Call us today to get the facts.  Call Toll Free 1-866-777-2557 or fill out our online contact form below and a Nebraska Stryker Hip Implant Lawyer will get back to you as soon as possible.   This is a free, no obligation consultation. There are no legal fees unless we make a recovery for you.  Time is limited, so please call today.











Stryker Hip Replacement Lawyer Nebraska









































We are investigating cases involving:

DePuy ASR Hip Recall
DePuy Pinnacle Hip Lawsuit
Wright Conserve Hip Cup
Wright Conserve Plus Lawsuit
Zimmer Durom Cup Hip Implant
Smith & Nephew R3 Acetabular System
Wright Profemur Z Hip Replacement
Stryker Rejuvenate

Stryker ABG II Modular Neck Stems

​Stryker LFIT Anatomic V40 Femoral Head
Metallosis

Cobalt Poisoning

Chromium Poisoning



FAQ


After finally deciding to undertake hip replacement surgery, a large number of patients have thoughts on the subject of their forthcoming hospital stay as well as the process of recovery that's needed following the surgical treatment. While a hip replacement is definitely a significant invasive process, improvements in medicine have augmented the safety/efficiency of a complete hip replacement. In fact, specialists might even be capable to perform the hip replacement using minimally-invasive surgical procedures.


Stryker Hip Lawyer Nebraska


FDA Not Suggesting The Utilization of Metal-on-Metal Hip Replacements
Lately, metal-on-metal hip implant models were being affected by a large number of recalls along with heightened patient troubles upon the safeness of such models. Various top manufacturers of these devices, such as Stryker, DePuy, and Smith & Nephew, have recalled its metal-on-metal hip implants and today face litigation through patients looking for settlement associated with sufferings resulting from these medical devices.


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On a metal-on-metal hip implant product, the parts in the product are constructed from several metals - most commonly, a cobalt-chromium-molybdenum alloy mixture. As the surfaces and conjunctions on the metallic components rub with each other, tearing apart of the areas will launch metal debris into the joint space. Early signs of this concern consist of excessive joint ache along with restricted movability.


With major conditions, such metal debris can cause a condition known as metallosis (metal positioning). This takes place once chromium or cobalt ions go into the individual's blood flow and also create a systemic response to the toxic volumes of metal. For majority of such people, complicated revision operation is the only alternative to get alleviation of the signs and symptoms of metallosis.

Stryker Hip Lawyer Nebraska


FDA Suggestions for Metal Hip Implants
The FDA has addressed consumer problem with the hazards of metal-on-metal hip alternatives, and also they have launched numerous safety warnings pertaining to these systems. Moreover, the FDA has come up with specific recommendations for orthopedic surgeons as well as individuals who have acquired a metal-on-metal hip enhancement. These advises feature:


• Regular clinical evaluation - with more constant consultations involving symptomatic clients
• Soft tissue imaging with people experiencing complications with their implant
• Metallic ion testing on symptomatic clients employing a metal enhancement
• Averting the employment of metal-on-metal enhancements with certain groups which have enhanced risk
• Extensive client counseling over the hazards of metal augmentations before surgery

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There are certain groups of patients which reports have shown an excessive probability of developing troubles when utilizing a metal hip alternative. Consequently, the FDA implies that doctors do not put up this form of model over these patients. Greater risk populations comprise of individuals with severe renal deficiency, metal sensitivity, and also suppressed immunity defenses. Also, metal enhancements could not be advised for utilization in females with childbearing age.


Even though individuals are not going through difficulties associated with metal-on-metal hip enhancements, the FDA advises that all patients with a metal enhancement follow-up upon their orthopedic specialist every one to 2 years in order to be assessed with complications. For clients who are displaying primary symptoms of metallosis or other complications, the FDA suggests that a clinical evaluation take place at least every six months.

Stryker Hip Replacement Lawyer NE