Stryker Rejuvenate Hip Recalls
Stryker Rejuvenate Hip Recalls
Hip replacement surgery is an ordeal in itself without the added risk of further complications down the line. Many in need of hip treatment received the Stryker Rejuvenate Hip Replacement System implant in hopes of regaining normal mobility function, but this was not the case. Stryker Rejuvenate Hip Recalls on the Stryker hip implant have led many to seek out legal counsel through Stryker hip recall lawyers. Understanding the complications caused by this implant device can help you decide whether you should seek further counsel to protect your rights.
The Stryker Rejuvenate Hip Replacement System
The Stryker Rejuvenate Hip Replacement System was advertised as more durable than its competitor models because of its sophisticated design. Unlike other designs, the Stryker model consists of several modular neck and stem components as opposed to the one-piece neck and stem design used by its competitors. This complexity was intended to allow for a more custom-fit during surgery. The metal materials used in the making of the implant were also advertised as superior to its competitor models, many of which were known to corrode and cause metal poisoning within three years time.
The Stryker Rejuvenate hip implant received FDA approval to market in June 2008. Because the device was similar in design to other devices on the market, no human testing was done prior to its approval. This, in part, accounts for the unforeseen complications so many people suffered after having the device implanted.
Stryker Rejuvenate Recalls
By 2012, reports of complications caused by the Stryker hip implant became a cause of concern for the manufacturer, which led to Stryker Rejuvenate Hip Recalls by mid-year. An increasing number of implant recipients were filing lawsuits against the manufacturer for marketing a defective product design.
In April 2012, the manufacturer issued an urgent safety alert to the public as well as to surgeons and hospital risk managers. Stryker manufacturers warned of the potential for the metal components that make up the device to corrode due to friction caused by moving parts. In effect, the likelihood of corrosion placed implant recipients at risk of metal poisoning.
In response to ongoing concerns surrounding the effects of the Stryker implant, the manufacturer issued voluntary Stryker Rejuvenate Hip Recalls of the device in June 2012.
Stryker Hip Recall Problematic Symptoms
- Inflammation and swelling
- Severe joint pain
- Difficulty walking and standing
Most, if not all of the symptoms result from the body’s immune system response to corroded metal materials at the implant site. Over time, metal materials can cause bone and tissue deterioration. Metal contaminants can also enter the person’s bloodstream.
After a certain degree of erosion has taken place, the implant itself can become dislocated and eventually breakdown altogether. At this point, implant recipients are facing the high likelihood of undergoing hip revision surgery to correct problems caused by the Stryker implant.
Stryker Rejuvenate Hip Recalls and Health Risks
Health risks you may encounter from a Stryker implant procedure can take the form metallosis and significant bone deterioration. Metallosis or metal poisoning happens when metal contaminants enter your bloodstream. Once in the blood stream, these materials can cause problems in other areas of the body, such as the nervous system, the heart and the thyroid gland.
Since older individuals are more likely to receive a hip implant, complications involving bone damage are common. In cases where hip revision surgery becomes necessary, surgeons must replace the existing implant with another one. Considering the damage that’s taken place, these surgeries are even more complicated than the original surgery since doctors have less actual bone material with which to work. As a result, patients face a long hard recovery period as the affected area heals.
Lawsuits & Settlements
In April 2013, the implant manufacturer entered into mediation hearings with a Stryker hip recall lawyer to settle pending lawsuits in the state of New Jersey. This was done in an attempt to head off the thousands of lawsuits filed against the company. New Jersey has already moved all Stryker Rejuvenate hip recall hearings to the Superior Court level in an effort to centralize the proceedings.
As of May 2013, plaintiffs involved in federally-filed Stryker lawsuits have petitioned for a Multidistrict Litigation suit. If granted, all Stryker Rejuvenate implant cases will be heard as one mass tort case within a single U.S. District Court.
The American Injury Attorney Group
No matter how air-tight a case may seem, without proper legal representation in the courtroom, you can greatly weaken your odds of getting what you rightly deserve. Stryker Rejuvenate Hip Recalls lawyers can offer the type of experience and expertise needed to ensure you receive the compensation you deserve.
The American Injury Attorney Group and its affiliates have a long track record in handing medical product recall cases. As specialists in this area, our team of lawyers fights on your behalf for compensatory damages and also for punitive damages. If you or someone you know has been affected by a faulty Stryker Rejuvenate hip implant, feel free to contact our office for a consultation and we’ll take it from there.