The Trouble with Stryker Hip Implants

Stryker Hip Implants has been an implant that’s come under scrutiny for the number of cases where patients are suing them because their hip replacement failed. Stryker is one of many companies being sued by these implants, which have led to extremely negative publicity when it comes to consumer safety. With a new CEO and discontinuing use in 2008, what will become of this struggling company?

The “stryker hip recall payouts 2020” is a legal issue that has been in the news recently. The Stryker Hip Implants were recalled after it was found that they were causing serious injuries and pain to patients.

The Trouble with Stryker Hip Implants

Stryker Orthopaedics has issued a hazard advisory for seven versions of Stryker V40 femoral heads used in metal-on-metal (MoM) hip replacement surgeries, alerting physicians and patients about possible adverse effects.

Many health groups have issued warnings as a result of these practices. Patients who had significant side effects and/or had to undergo revision surgery as a consequence of MoM problems have filed hundreds of cases.

Stryker must be held accountable.

The following are among of the negative effects mentioned in the most current Stryker alert:

  • Impairment of mobility
  • Pain
  • Inflammation
  • Tissue response that is not good
  • Dislocation
  • 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.

Because of the concerns indicated in the advisory, several businesses have stopped making MoM hip implants entirely. Metal particles may be discharged into the bloodstream when the metal head grinds against the metal socket, causing cobalt chromium poisoning.

As a consequence, since 2010, pharma and health organizations all throughout the globe have issued cautions concerning MoM substitutes.

The FDA and other government agencies have issued a warning about “unique risks.”

“In addition to the basic dangers of all hip implants, metal-on-metal (MoM) hip implants have particular concerns.”

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.

A $1.4 billion settlement has been reached over Stryker hip implants.

Given the alarming health hazards identified by the FDA, MHRA, Health Canada, and Stryker, a Rhode Island court recently dismissed Stryker’s attempt to dismiss a case involving their Trident hip replacement system.

In truth, the company is no stranger to legal issues. 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.

Please call us immediately away if you have suffered from metal poisoning, dislocations, discomfort, inflammation, or shattered bones and need revision surgery as a consequence. You may be eligible for compensation for medical costs and other expenditures incurred as a result of your device’s unanticipated adverse effects if you file a lawsuit.

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Stryker Hip Implants has been a problem for some patients in the past. The company was recently fined $1.5 billion dollars because of this issue. Reference: stryker hip replacement 2019.

Frequently Asked Questions

How long do Stryker hips last?

A: Stryker hips last approximately 3-5 years. They are made of a light plastic and cannot handle long use without breaking or becoming misshapen.

Are there any recalls on Stryker?

A: At this time, there are no recalls on Stryker.

What are the signs of a failing hip implant?

A: Some signs of a failing hip implant might include a feeling that the hip is not moving as it used to, and pain during movement.

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