Attorney at Graves McLain Injury Lawyers

Practice Areas: Car Accidents, Medical Malpractice, Vaccine Injuries

When a hip replacement implant doesn’t work as expected—or is recalled—it can lead to severe pain, health complications, or the need for additional surgery. For many patients, learning that their device has been recalled raises difficult questions about what happens next.

This blog explains how hip implant recalls work, why some devices are removed from the market, and what patients should do if their implant is part of a recall. Whether you’re already experiencing complications or want to understand your options, knowing the facts can assist you in making accurate choices on your health and legal rights.

What Is a Medical Device Recall?

A medical device recall is a formal process that corrects or removes a device that may cause harm or violate safety rules. These recalls are either initiated by the manufacturer or mandated by the U.S. Food and Drug Administration (FDA).

The FDA defines a medical device recall as a correction or removal of a product that violates the laws it enforces and presents a risk to health.

In the case of hip implants, a recall may involve fixing the device, changing the labeling, or stopping sales altogether. If the implant is already in a patient’s body, it doesn’t always mean it must be removed. Sometimes, it’s safe to monitor the device rather than replace it, depending on individual risk.

Why Are Hip Implants Recalled?

Hip implants can be recalled for several reasons, often tied to product defects or safety concerns discovered after the device was implanted in patients. These problems can lead to pain, injury, or revision surgery.

Some of the most common reasons include:

  • Loosening of the implant
  • Premature wear and failure
  • Squeaky or grinding joints
  • Dislocation or bone fracture
  • Metal ion release, also called metallosis

Many recalled hip implants were metal-on-metal designs, which have been linked to metallosis, a condition where metallic debris builds up in the body and causes severe tissue damage.

Implants made with metal components can corrode over time, releasing particles into the bloodstream. This can trigger immune reactions, pain, tissue damage, and even permanent mobility loss if not addressed early.

The FDA’s Role in Hip Implant Recalls

The FDA oversees the recall process to ensure patient safety and hold manufacturers accountable. When a manufacturer becomes aware of a serious issue, they’re expected to recall the device and notify the FDA voluntarily. In some cases, the FDA can step in and enforce the recall directly.

Recalls are classified into three levels based on the risk to patient health:

FDA Recall Classification Table

Recall Class

DefinitionRisk Level

Example in Hip Implants

Class IReasonable chance of serious health consequences or deathHighDePuy ASR hip system recall
Class IIMay cause temporary or reversible health consequencesModerateStryker Rejuvenate modular stem
Class IIIUnlikely to cause adverse health consequencesLowLabeling or packaging errors

In a 2022 update, the FDA noted that “Class I recalls represent the highest risk level, demonstrating a plausible risk of mortality or significant adverse health effects.

Recalls are published in the FDA Medical Device Recall Database and listed in weekly enforcement reports to keep the public informed.

Primary Hip Implant Recalls in Recent Years

Several hip replacement systems have been removed from the market over the years. Some of the most well-known include:

  • DePuy ASR and Pinnacle systems
  • Stryker LFit V40 femoral heads and Rejuvenate stems
  • Zimmer Biomet M/L Taper with Kinectiv Technology

According to a 2023 report from the Journal of Patient Safety, hip implant recalls increased by nearly 25% over the previous five years, primarily due to premature failure and metal toxicity risks.

These recalls have led to lawsuits from patients harmed by defective implants. While many manufacturers have agreed to settlements, legal claims vary by case. It’s essential to speak with an attorney who understands product liability law before deciding your next step.

What Should You Do If Your Implant Was Recalled?

If you learn that your hip implant is on a recall list, don’t panic—but don’t ignore it either. Not every recalled device must be removed. The response depends on your health, the device’s condition, and your doctor’s advice.

Here’s what you should consider:

  • Speak with your orthopedic surgeon- Ask if your specific device was recalled and whether your symptoms require follow-up care.
  • Watch for signs of failure- These include pain, swelling, instability, or strange sounds coming from the joint.
  • Request imaging or blood tests- Your doctor may test for elevated metal levels or look for tissue damage around the implant.
  • Know your legal rights- If the recalled device caused harm, you may be able to file a claim for medical bills, pain, or other losses.

Each situation is unique. A trusted legal team can help review your records and determine if you may qualify for a case.

How Graves McLain Injury Lawyers Can Help

Graves McLain Injury Lawyers has represented clients across Tulsa and Oklahoma who defective medical devices have harmed. If your hip replacement has been recalled and you’re dealing with pain, revision surgery, or disability, you don’t have to face the aftermath alone.

Our team understands how complex medical product liability cases can be. We offer legal guidance and case evaluations to help patients explore their options and take action if needed.

Frequently Asked Questions

What does it mean when a hip implant is recalled?

A recall means the device has been found to violate safety regulations. It may pose a health risk, require correction, or be removed from the market.

Do all recalled hip implants need to be removed?

Not always. Your doctor may recommend monitoring, adjustments, or surgery depending on the severity and symptoms.

How do I find out if my implant has been recalled?

You can search the FDA Medical Device Recall Database or speak with your orthopedic surgeon for device details.

What are the symptoms of a failing hip implant?

Common signs include pain, swelling, instability, clicking sounds, limited mobility, or signs of metal poisoning like fatigue or rashes.

Can I file a lawsuit if my hip implant was recalled?

You may be eligible to file a legal claim if the recalled implant caused harm. A legal review can help assess your options.

What damages can be claimed in a hip implant lawsuit?

Potential damages may include medical expenses, revision surgery costs, pain and suffering, and lost wages. Every case is unique.

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Conclusion

Hip implant recalls are a serious matter. While not every recall leads to removal, patients deserve to understand their options, especially when facing unexpected complications or pain. Staying informed about recalls, knowing what symptoms to watch for, and seeking early legal guidance can help protect your health and your future.

If your implant has been recalled or you suspect something is wrong, speaking with an experienced attorney at Graves McLain Injury Lawyers can help you take the next step. Every situation is different, and the proper guidance can make all the difference in understanding your rights and pursuing justice.

When injury victims need a law firm with a reputation for excellence, turn to Graves McLain Injury Lawyers. We are a top-rated personal injury firm determined to be the best. With decades of award-winning representation, our clients recover the compensation they need to put their lives back together.

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  • My orthopedic doctor recommended Graves McLain Injury Lawyers, PLLC, to me following the need for revision hip surgery due to a hip from Stryker that was putting poison into my system. The doctor took care of the hip, and Graves McLain Injury Lawyers, PLLC, took care of the legal case. They were very thorough, professional, courteous, and always ready to answer the questions I had throughout the length of the case. In a word, the entire office is fantastic. I’m sure they were tired of my inquiries on the case’s progress, but they did not show it. They were always willing to respond and were very positive. If I ever have a claim in the future, they will be the first group to whom I reach out.

    Robert S.

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