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Posts Tagged ‘Stryker Rejuvinate modular-neck stem hip implant’

Stryker Hip Replacement Recall Lawsuits Continue To Proceed

Written by lisaspitzer on . Posted in Depuy Hip Replacement Blog, Stryker Hip Replacement, Stryker Hip Replacement Lawyer

Stryker hip recall lawsuits are moving forward in a consolidated litigation established in New Jersey Superior Court, Bergen County .   Judge Brian R. Martinotti has scheduled the litigation’s initial conference for February 20, 2013 at 10:00 a.m. (In re Stryker Rejuvenate Hip Stem and the ABG II Modular Hip Stem Litigation, No. 296 (N.J. Super. Ct., Bergen Cty.)

Both the Stryker Rejuvinate Stem and ABGII Modular Hip Stem were recalled and the hip replacement helpline Stryker division has had numerous calls from people suffering from a failed Stryker metal component hip replacement.

On January 17, 2013, the FDA issued a safety communication regarding metal-on-metal hip implants. The press release is an update to the agency’s evaluation of the potential complications of these devices. The update notes that all-metal implants carry risks that are unique because of the friction of their components.

Stryker has claimed the new hip replacement would:

  • Rejuvenate hips were first made available by Stryker in February 2009
  • increased stability,
  • better mobility,
  • superior fit over other hip replacement implants on the market.

Apparently this is not the case as it was necessary to recall the implants and lawsuits are flooding in. Get an experienced Stryker lawsuit Lawyer at the Stryker Hip Replacement Help division of Hip Replacement Helpline

Thousands of people have been filing Stryker Hip Replacemant lawsuits like Laray Johnson, a resident of Alabama. He received a Stryker Rejuvenate implant in his right hip on March 22, 2011. He then received a Rejuvenate implant in his left hip on June 24, 2011. This was a year prior to the voluntary Stryker hip recall. Mr Johnson began to experience substantial pain and discomfort around the area of the implants.

Thousands are filing lawsuits and we hear from many every day with telling us about  device deterioration and corrosion,  serious problems, bone fractures, metallosis, tissue damage, and severe pain.

Call us for a Stryker lawyer today.

Stryker Hip Replacement Lawsuit Update, Stryker Hip Replacement Lawyers

Written by lisaspitzer on . Posted in Depuy Hip Replacement Blog, Stryker Hip Replacement, Stryker Hip Replacement Lawyer

Stryker has recently recalled it’s Rejuvinate Hip replacement and ABG II Hip Stems due to the number of failed components causing complications. In June 2012, Stryker initiated a voluntary recall of its Rejuvenate and ABG II modular-neck hip stems. “While modular-neck hip stems provide surgeons with an option to correct certain aspects of a patient’s anatomy and hip biomechanics, we decided to voluntarily recall these modular-neck hip systems due to the potential for fretting and corrosion at the modular-neck junction which may result in ALTR (adverse local tissue reactions), as well as possible pain and/or swelling at or around the hip.” Since that date we have had  100’s of calls from people with a failed hip replacement.

The DePuy Hip Replacement Helpline announces The Stryker Hip Replacement Helpline. The mission of the new Stryker Hip Replacement Helpline is to locate all people with a failed Stryker who have required revision surgery or have been told they need revision surgery and help them file a Stryker Hip Replacement lawsuit.

New Jersey Stryker Lawsuit Update

The New Jersey Supreme Court has ruled that all cases in the state should and will be consolidated into a “multicounty litigation” in Bergen County Superior Court before Judge Brian R. Martinotti.

Stryker Hip Replacement Helpline  lawyers are filing lawsuits for injury from the newly recalled Stryker Rejuvinate Hip Replacement and ABG II Modular Stems.

A number of  patients with failed metal component  hip replacements have chosen  to file a Stryker hip replacement lawsuit after experiencing serious complications linked to the devices, and a consolidation of a number of lawsuits has taken place.

If you have been injured by a Stryker Rejuvinate Hip replacement recall  or the ABG II Modular Stems  we want to hear from you and  connect you to a  lawyer to review your medical records to see if you have a claim against Stryker for your failed hip replacement.

 

Stryker Helpline Launches National Campaign To Locate Seniors With Recalled Stryker

Written by lisaspitzer on . Posted in Stryker Hip Replacement

Learn About Your Stryker Hip Replacement

Many seniors have fallen victim to the new Stryker hip replacement recall. This is not metal on metal but, Metal stems and components but, has shown the same rate of complications and metal toxicity factors. Seniors must see a doctor immediately and contact our Stryker helpline for a lawyer. Revision surgery for seniors includes months of rehabilitation. Our concern for our seniors with these faulty hip replacements has lead to a massive outreach campaign to contact all seniors with this implant and their families and children to be alerted to the potential need for revision surgery and to learn about the current Stryker lawsuits.
IN July of  2012 Stryker Orthopaedics recalled the Rejuvenate Modular Hip System and ABG II Modular-neck stems due to risk of wear and  corrosion resulting in the need for additional  revision surgery.

Stryker Implant Failure is Hurting Many Seniors

We urge seniors to contact the Stryker Implant Helpline asap to get information regarding  the  early failure of the device  and the need for revision surgery

  •     Wear and corrosion at the modular-neck junction
  •     Osteolysis or bone dissolution
  •     Joint loosening and dislocation
  •     Excessive metal debris leading to metal  toxicity
  •     Inflammation of tissues
  •     Death of tissues
  •     Pain
  •     Allergic responses
  •     Broken device
  •     Adverse Local Tissue Reaction

 

 

 

Stryker Lawsuit Updates, Stryker Lawyers Propose Consolidation

Written by lisaspitzer on . Posted in Depuy Hip Replacement News

Current news and updates regarding the Stryker Hip Replacement

Consolidation Of Lawsuits Against Stryker Are In the Works
The Logic Behind The Consolidation

Lawsuits have been filed against Stryker Orthopaedics over its defective hip implants.  Cases are under consideration for consolidation New Jersey.The  The proposal is to move for an MDL or consolidation in Bergen County Superior Court in Hackensack, N.J., Honorable Brian Martinotti, who is the judge presiding over that court, has experience overseeing Depuy ASR hip implant lawsuits.

At issue are Stryker’s Rejuvenate and ABG II modular-neck hip stems, which were marketed as a way for orthopaedic surgeons to give patients a better fit with their hip implants because they can be customized using various parts. The Rejuvenate hip offers surgeons six stems and 16 necks, and the ABG II has 10 necks and 16 stems that work together.
Metal-on-Metal Problems

The problem, however, is that the neck and stem parts have all-metal conjunctions, Stryker stated, which are to blame for complications similar to those seen in DePuy hip implant patients. Stryker patients are experiencing painful, early failure of their devices because the metal parts are grinding against each other and wearing out. Most hip implants have an average life of 15 years, but the Rejuvenate and ABG II modular-neck hip stems are failing after just months, by some reports. All-metal hip implants also have been associated with metallosis, or the poisoning of the bloodstream.

Stryker recalled the Rejuvenate and ABG II on July 6, 2012. The Rejuvenate had only been on the market since February 2009.

If you have a failed Stryker Implant contact the helpline today.

Stryker Hip Implant Recalls, Stryker Hip Replacement Lawyers

Written by lisaspitzer on . Posted in Depuy Hip Replacement Blog

Hip replacement lawyers are accepting clients for the The Stryker ABG II modular-neck stem used for total hip replacement surgery and
The Stryker Rejuvinate modular-neck stem hip implant. Stryker recalled both of these products on July 4, 2012 because the metal of the neck and stem can corrode, releasing toxic metal ions that can damage tissue and bones around the hip implant.  This can cause severe pain, inflammation, metal poisoning (metallosis from chromium and cobalt), tissue death (necrosis), bone damage, pseudotumers, gait issues, and other serious problems. Revision surgery (to remove and replace the recalled Stryker hip product) may be required.

Hip Replacement Lawyers and the DePuy Hip Replacement Helpline has launched a special division and helpline for victims of a failed Stryker hip implant.

Styker Orthopaedics has announced a recall of the ABG II modular-neck stem hip implant. Metal-on-metal parts of the device can corrode, shed toxic nano-particles into the body, and cause severe pain, inflammation, metal poisoning (metallosis), pseudotumors, and more
What You Can Do & How a Stryker ABG II Hip Implant Lawsuit Can Help

The Stryker ABG II modular-neck stem

The Stryker ABG II modular-neck stem is a new type of multi-piece hip replacement system. When it was approved, the company claimed that its many interchangeable parts made it ideal for matching each patient’s unique biomechanics.
Although the Stryker ABG II is technically a plastic-on-ceramic hip implant, the device has a unique neck/stem junction that is a metal-on-metal design. Like other metal-on-metal hip implants (including the DePuy ASR, which was recalled in 2010), the Stryker ABG II was fast-tracked through the FDA’s approval process via the 510(k) system. The FDA allows manufacturers to avoid conducting long-term safety studies of new devices so long as they are “substantially similar” to existing devices
Stryker ABG II Recall

Stryker first warned orthopedic surgeons about the risks of the ABG II hip implant in an Urgent Field Safety Notice that was sent in May 2012. The warning advised doctors to be aware of the following severe side effects associated with the ABG II hip implant:

  •     Excessive corrosion at the neck joint, which could shed toxic nano-particles into the patient’s body
  •     Pain, inflammation, tissue damage, and swelling caused by toxic metal nano-particles
  •     Allergic reaction, especially in patients with metal sensitivity
  •     Osteolysis (dissolving bone loss) caused by metal nano-particles

Complications

  •     Chronic pain in the hip joint
  •     Inflammation, swelling
  •     Less walking ability, changes in gait
  •     Metallosis (metal poisoning)
  •     Corrosion of the hip implant
  •     Tissue damage or death (necrosis)
  •     Bone loss in the hip
  •     Pseudotumors

The Stryker Rejuvenate hip implant

Stryker Rejuvenate Recall
In July 2012, Stryker voluntarily recalled its Rejuvenate and ABG II modular-neck stems from the market. The products were recalled due to reports of fretting and corrosion. According to some reports, the FDA received two adverse events linked to the recalled devices, including one in which the device was removed.

On May 28, 2012, Health Canada announced that Stryker Rejuvenate was being recalled so the instructions for use could be updated. The recall affected only Rejuvenate devices sold in Canada and was based on a reported rate of less than one percent for revisions associated with the Rejuvenate. So far, no such Stryker recall has been announced in the US.

Call the Stryker hip implant helpline for a Stryker hip replacement Lawyer Today