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Stryker Hip Lawyer Minnesota - Stryker Hip Replacement Lawyer Minnesota

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 Minnesota 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 MN

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

Stryker Hip Lawyer Minnesota

FDA Does Not Encourage the Use of Metal-on-Metal Hip Solutions
In recent times, metal-on-metal hip implant products were being affected by a lot of recalls and also substantial client distress with the safeness of such devices. A few major producers of these systems, consisting of Stryker, DePuy, along with Smith & Nephew, have ordered back their metal-on-metal hip enhancements and face legal cases today through clients searching for payment associated with injuries attributable to these products.

Stryker Hip Lawsuit Minnesota

With a metal-on-metal hip implant model, the pieces in the product are constructed from a variety of metals - most often, a cobalt-chromium-molybdenum alloy blend. When the surfaces as well as conjunctions with the metallic components rub with one another, tearing apart on the areas would discharge metallic debris to the joint area. Primary indications of this condition consist of excessive joint soreness as well as limited transportability.

Stryker Hip Lawyer Minnesota

In significant circumstances, the metallic debris can cause a condition known as metallosis (metal poisoning). This happens if chromium or cobalt ions get into the client's blood circulation and also result in a systemic reaction to the toxic levels of metal. For many of these individuals, intricate revision surgical procedure is the only option to obtain alleviation of the symptoms regarding metallosis.

FDA Recommendations for Metal Hip Enhancements
The FDA has resolved individual distress about the dangers of metal-on-metal hip replacements, and have launched numerous safety warnings concerning these models. Additionally, the FDA has put together specific recommendations for orthopedic surgeons and people who have received a metal-on-metal hip enhancement. Such recommendations comprise of:

• Frequent medical examination - with additional constant consultations for symptomatic patients
• Soft tissue imaging with individuals experiencing issues with their augmentation
• Metallic ion testing in symptomatic clients using a metal enhancement
• Fending off the use of metal-on-metal implants for particular demographics that have increased risk
• Extensive client advices upon the hazards of metal augmentations before surgery

Stryker Hip Recall Lawyer Minnesota

There are particular groups whom researchers have shown to have an increased risk of developing difficulties with a metal hip alternative. Thus, the FDA endorses that specialists should not attach this form of model over these patients. Greater risk demographics contain patients with extreme renal inadequacy, metal sensitivity, and also suppressed immunity defenses. Also, metallic enhancements will not be suitable for utilization in females with childbearing years.

Stryker Hip Replacement Lawyer MN

Even though individuals are not encountering issues connected with metal-on-metal hip augmentations, the FDA recommends that each client with a metal enhancement follow-up over their orthopedic doctor within 1 to two years to be screened for troubles. For those patients that are demonstrating primary symptoms of metallosis or other difficulties, the FDA endorses that a medical evaluation happen at least every six months.

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