The hip implant market is the largest in the world, with over 100 million surgeries performed yearly. The US FDA has regulated implants since 1980 and it’s responsible for preventing adverse events like infections or metal debris. Despite this regulation, there have been thousands of lawsuits filed against manufacturers alleging safety issues associated with their products.
Stryker Hip Implant Recalls & Settlements – Hip Replacement Lawyers is a blog post that discusses the stryker hip implant recall. The article includes information about the settlement, the lawsuits, and other important information for those who may have been affected by this issue.
Several metal-on-metal (MoM) hip implants manufactured by Stryker Orthopaedics have failed to work properly, resulting in widespread recalls and litigation. Stryker is the company that made the Rejuvenate and ABG II hip stems, which were both recalled.
Stryker has a history of producing metal-on-metal (MoM) hip implants that don’t work properly, resulting in widespread recalls and litigation.
Stryker agreed to pay $1.43 billion to resolve hundreds of complaints over its ABG II and Rejuvenate hip replacements in the autumn of 2014. Each plaintiff might collect up to $600,000 in damages under the terms of the agreement.
Stryker’s V40 femoral heads (used in MoM hip replacements) now look to be dangerous enough to merit a corporate notice warning of possible adverse effects include loss of mobility, discomfort, inflammation, and dislocation.
If you had a Stryker hip implant and had unanticipated adverse effects that necessitated revision surgery, please contact us straight away to learn about your options. You could be eligible for a lawsuit to help you pay for medical bills and other costs associated with your Stryker equipment.
Stryker Orthopaedics is a company that specializes in orthopaedics.
In February 1946, Dr. Homer Stryker created The Orthopedic Frame Company (which would later become the Stryker Corporation) in Kalamazoo, Michigan. Dr. Stryker was an orthopedist and inventor who, among other things, invented the mobile hospital bed, the oscillating saw (a cast-cutting instrument), and the walking heel.
His firm went public in 1977. It bought the Osteonics Corporation, which made hip, knee, and other orthopedic replacements, in 1979. Dr. Stryker died the next year, at the age of 85, in 1980. The corporation would be run by his offspring and grandkids.
Stryker purchased Pfizer’s orthopaedic subsidiary, Howmedica, in 1998 and renamed it Stryker Orthopaedics. (This is one of the company’s around two dozen big purchases during the last 20 years.) Stryker Corp.’s yearly revenues reached $2 billion in 1999. They surpassed $3 billion in 2002. Nearly $5 billion was spent in 2005.
Stryker Corp. employed more than 20,000 employees throughout the globe in 2015, with annual revenues of $10 billion.
“Unique Risks” are associated with metal-on-metal hip implants.
The problem with metal-on-metal (MoM) hip implants is that metal particles may be discharged into the bloodstream when the metal ball and socket rub against each other, causing cobalt chromium poisoning. As a result, numerous orthopedic businesses have stopped making MoM implants.
Furthermore, health organizations from all around the globe have voiced worry about these implants.
The Medicines and Healthcare Products Regulatory Agency (MHRA) in the United Kingdom issued a warning concerning MoM hip replacements in the spring of 2010. The MHRA encouraged people to obtain blood testing and imaging to make sure they weren’t poisoned by metals. The MHRA followed up two years later with recommendations for monitoring and caring for MoM hip patients.
In 2012, Health Canada issued an advisory to MoM hip replacement surgeons and patients with significant safety information. This warning stated:
Increasing amounts of metal (cobalt and chromium) ions in the surrounding joint tissue have been linked to increased degrees of discomfort, implant loosening, and substantial soft tissue responses in recent years. Soft tissue responses may vary from minor fluid collection to more serious necrotic and “pseudotumor” reactions, necessitating device replacement.
“Soft tissue responses were seen in 14.2% of updated MoM hip implants,” according to Health Canada.
“Metal-on-metal (MoM) hip implants have particular dangers in addition to the basic risks of all hip implants,” the US Food and Drug Administration (FDA) notes on its website under the Metal-on-Metal Hip Implants section.
If a patient is having symptoms that indicate their implant isn’t working properly, the FDA recommends taking the following steps:
- Aspiration of the joints (removing fluid from around the joint)
- Imaging of soft tissues
- Metal ion levels are checked in blood testing.
According to the FDA, MoM hip implant patients should be extremely cautious about their overall health, since some medical research shows that MoM hip implants might cause systemic responses elsewhere in the body.
Skin rash and hypersensitivity, cardiomyopathy, neurological abnormalities, renal function impairment, depression or cognitive impairment, and thyroid malfunction are all possible side effects.
Stryker Issues a Hazard Alert for the Accolade V40
Stryker Orthopaedics issued a hazard advisory in October 2016, advising clinicians and patients about the possible negative effects of seven variants of Stryker V40 femoral heads used in metal-on-metal (MoM) hip replacement surgeries.
The following are some of the negative effects listed in the Stryker alert:
- Impairment of mobility
- Tissue response that is not good
- Instability of joints
- Bones are broken.
- Disparity in leg length
- Revision surgery is required.
Despite the fact that the advisory is not technically a recall, it may deter surgeons and patients from opting for complete hip replacements using a Stryker V40 femoral head.
In Canada and Australia, the Accolade V40 has been recalled. Even Nevertheless, this possibly faulty femoral head is used in an estimated 44,000 hip implants worldwide.
Stryker Pays $1.4 Billion to Resolve Hip Implant Lawsuits
Stryker issued a recall in 2012 for two metal hip implants, the Rejuvenate Modular and ABG II Modular-Neck hip stems. Concerns that the pieces would fret or corrode, causing discomfort, swelling, and inflammation in the surrounding tissue prompted the business to take action.
Stryker settled complaints over its ABG II and Rejuvenate hip stems for $1.43 billion.
The recalled neck stems are suspected of causing major health concerns including discomfort and inflammation, early hip implant failure, and metal poisoning, which may lead to systemic difficulties affecting the heart, neurological system, and thyroid.
Thousands of patients filed complaints after the Stryker recalls in 2012, many of whom would have to face yet another arduous surgery and recuperation as a result of a faulty implant.
Stryker agreed to pay $1.43 billion to resolve complaints over its ABG II and Rejuvenate hip stems in the autumn of 2014. Each plaintiff might collect up to $600,000 in damages under the terms of the agreement.
A Texas jury awarded $1 billion to six plaintiffs who required revision procedures due to unpleasant side effects from their DePuy Pinnacle hip implants in a similar action in December 2016. (DePuy is a Johnson & Johnson company.)
You Might Be Eligible For Reimbursement
If you or a loved one has suffered metal poisoning, dislocations, discomfort, inflammation, or shattered bones as a consequence of a defective hip implant, please call us immediately away to learn about your options.
You may be eligible for a lawsuit to collect medical costs, lost earnings, and other expenditures incurred as a result of your device’s unanticipated negative effects.
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Stryker Hip Implant Recalls & Settlements – Hip Replacement Lawyers. Stryker is recalling 2020 hip implants and offering settlements to those who have received them. Reference: stryker recall 2020.
Frequently Asked Questions
What hip implants have been recalled?
A: There have been a few hip implants recalled, but I cannot answer this question.
Are there any recalls on Stryker?
A: There are no recalls on Stryker.
Are Stryker hip replacements safe?
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