Pennsylvania Stryker Hip Replacement Recall Lawsuits
Due to higher than expected complaints of taper lock failures, Stryker may announce a new hip implant recall concerning select LFit V40 femoral heads in the very near future. These shortly to be recalled Stryker hip implant femoral heads are considered to be used on both Accolade 2 and Accolade TMZF in addition to Meridian and Citation stems. Risks from these malfunctions include: Disassociation of femoral head from hip stalk, Fractured hip stalk Excessive metallic debris, trunnion and numerous other complications.
Along with the LFit V40 failures, the medical device business Stryker is facing thousands of lawsuits from those who have suffered complications from ABG II hip implants and the business’s Rejuvenate. You should join these individuals to seek the settlement you deserve to ensure the greatest healing from this distressing ordeal, if you or a loved one was hurt by one of these recalled hip implants.
Stryker Hip Replacement Suits Are Piling Up
The lawyers at The Feather Law Group have been at the vanguard of this litigation that was national by helping negotiate resolutions on behalf of wounded Americans. We understand faulty hip litigation cases inside and out. That’s why you should give us a call today if you or a loved one has suffered due to a defective ABG II or Rejuvenate hip replacement.
Time is exceptionally restricted to participate in this litigation, so don’t delay. There isn’t any cost or obligation on your own part to talk with us.
Stryker recalled ABG II modular and its Rejuvenate -neck hip comes in June 2012. The recall came after the devices were linked to high failure rates and corrosion of the joint’s metal components, which can damage surrounding tissue. Many individuals with one or both of these kinds of hip implants have had to undergo revision surgery to repair these issues.
Stryker Hip Complications
The pain related to a precarious hip replacement can be agonizing. Reports on file with the Food and Drug Administration tell of patients unable to walk and suffering other complications.
Complications connected with Stryker’s recalled Rejuvenate hip systems and ABG II comprise of:
- Joint pain, which frequently results in trouble walking.
- Metal poisoning, or metallosis. This happens when parts of the implant grind metal, sending metal shards into the body.
- Bone dissolution, or osteolysis. This can bring about implant failure or broken bones.
- Joint loosening or malfunction. Your hip cannot function as it should if the implant fails. This needs revision operation.
- Nercrosis, or tissue death. This may appear in the region encompassing the hip implant.
Are Individuals Suing Over Recalled Stryker Hips?
None of the plaintiffs in Stryker hip implant suits wanted to wind up in this scenario. All you and other hip victims wanted was a hip replacement that did its job.
The complications these recalled Stryker hips have caused are simply distressing. Additionally they put a tremendous mental, physical and financial burden on their families and patients. Addressing these hip complications frequently demands subjecting the patient to a revision operation – an expensive process with a long recuperation period.
If you are the victim of a defective hip, you don’t deserve this.
Nothing will take back the pain this ordeal caused. Nevertheless, requiring legal action may have the capacity to get you the resources you need to ensure the suffering ceases stops immediately.
According to a Wall Street Journal in October 2013, Stryker is estimated to have spent up to $1.13 billion to end the lawsuits that come from the recall of these two products.
What’s a Metal-on-Metal Hip Implant?
Metal-on-metal hip implants were initially promoted as a substitute to orthopedic implants coated with ceramic or plastic. Based on lab testing, the all-metal implants were demonstrated to be immune to wear and to reduce the danger of dislocation.
Yet it seems the apparatus are prone to early failure. Medical researchers have expressed concern over time about the security of metal-on-metal hip apparatuses due to effects of metal parts rubbing against each other. That’s why some hip systems by Stryker and other manufacturers have been recalled.
Patients who are at higher risk include, but are not limited to:
- Female patients
- Patients who are seriously overweight
- Patients with high degrees of physical action
Stryker released ABG II and its Rejuvenate in 2009, but recalled the apparatus three years after in July 2012. Stryker’s metal-on-metal hip implant started to demonstrate signs of corrosion after the apparatuses were planted.
It is often alleged that Rejuvenate hip systems and the ABG II weren’t adequately scrutinized before being approved for the marketplace.
Critics are calling on the FDA to shut this “loophole.”
Our Experienced Lawyers Need to Help
If you or a loved one received a Stryker hip implant and have experienced complications or have had to undergo revision surgery as a result, contact our Stryker hip implant lawyers today at the Greg Feather Law Group for a free case evaluation to learn about your legal options.
There is no obligation. Our attorneys will work closely with you to seek justice and fight for compensation for your injuries.