Cartiva Toe Implant Recall Lawsuits

Lawyers are now filing claims for those who suffered complications from defective Cartiva Toe Implants.

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Those who have suffered the following complications may be entitled to substantial compensation:

  • Severe pain
  • Nerve damage
  • Implant migration
  • Implant fracture
  • Repeat surgery.
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Our attorneys specialize in medical device litigation. "The free evaluation is always confidential."

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The Cartiva implant is a synthetic cartilage device intended to treat big toe arthritis that causes stiffness, pain and loss of mobility. This condition affects more than 2 million people and usually requires bone fusion surgery.

toe implant lawsuit

Cartiva Toe Implants Recalled for Failure Risks

The PVA hydrogel implant was designed to mimic the joint movement of natural cartilage, while resisting swelling and remaining compatible with human tissue. Approved by the FDA in 2016, it was marketed as a game-changing alternative to big toe fusion surgery. 

Although Cartiva’s product insert warned of a 13.5% failure rate, new evidence suggests it is drastically higher. This led Stryker to recall the implant in late 2024. However, reports show the company knew the risks for years, and should’ve recalled it before thousands of people were affected. 

Since Cartiva hit the market, the FDA has received over 150 reports of serious complications. Most of these involve the implant shrinking and movement. When it becomes loose or dislocated, the implant can cause significant nerve damage and pain, often leading to additional surgeries.  

Now, studies show that as many as 79% of Cartiva implants may fail within two years, with Cartiva patients requiring a second surgery almost 30 times as often as those who underwent other procedures. 

Due to Stryker’s failure to properly warn patients of the risks of Cartiva, lawyers expect those who’ve been affected may be entitled to substantial awards.

Do I Qualify for a Cartiva Lawsuit? Latest 2025 Updates

The Cartiva recall applies to all implant models and sizes sold since 2016. Experts have determined that the risk of failure outweighs any benefit to using the device over traditional fusion surgery. 

In addition to removing Cartiva from the market, doctors have been advised to monitor those patients who received the implants for complications such as:

  • Severe pain
  • Nerve damage
  • Implant dislocation or fragmentation
  • Swelling
  • Stiffness
  • Difficulty walking.

If you experienced any of these problems from your implant, or required repeat surgery on your toe, you may qualify for a lawsuit. Lawyers believe thousands of patients may be affected.  

The first Cartiva lawsuit trial is scheduled to start in October of 2025. However, victims may not have until then to file a claim in every situation. To ensure that your legal rights don’t expire, it’s recommended that you speak with a lawyer as soon as possible. 

For more information on the Cartiva lawsuits, or to discuss your case and legal options directly with a lawyer, contact DrugNews today.

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Timeline of Cartiva Lawsuits

Latest Information on the Cartiva Litigation

2025
Oct 25
First Cartiva lawsuit trial scheduled to begin.
2024
Oct 31
With mounting patient complaints and evidence of early failure, Stryker issues a recall for all Cartiva Synthetic Cartilage Implants sold since July 2016.
2024
Oct
King’s College Study reveals Cartiva recipients require repeat surgery nearly 30 times more often than toe fusion patients.
2020
Nov
Post-market studies raise concerns about Cartiva’s long-term performance. Reports from surgeons and patients suggest a failure rate as high as 64%.
2019
Wright Medical is purchased by Stryker for $4 billion.
2018
Cartiva is purchased by Wright Medical for $435 million.
2016
- 2023
The Cartiva toe implant is used in thousands of surgical procedures.
2016
The Cartiva toe implant receives FDA approval and is marketed as a revolutionary solution for maintaining mobility while reducing pain in the big toe joint.
2016
Motion Study sponsored by the manufacturer claims that Cartiva patients have less pain, fewer complications and greater function than fusion patients.
2011
Cartiva is founded in Alpharetta, Georgia to develop a synthetic cartilage implant aimed at treating osteoarthritis of the big toe joint.

Is There a Cartiva Class Action Lawsuit?

No. Lawyers expect thousands of victims will eventually file lawsuits against Stryker for complications or repeat surgeries due to defective Cartiva implants. However, claims are likely to be consolidated into special multidistrict litigation courts rather than a Class Action Lawsuit.

In order to handle the volume of cases most efficiently, lawsuits that claim similar injuries from one product, like Cartiva, are often consolidated into specific courts like these.  

Instead of forcing people into a single class action lawsuit for Cartiva injuries, multidistrict litigation (MDL) courts allow victims to band their individual cases together in a special court to seek damages against Stryker. 

This process offers more advantages to victims than class action lawsuits. In a class action, lawyers gather class participants together, who must then share whatever is awarded. However, individual participants in a MDL select their own lawyer, have more control over their case and whether it settles, and reap higher award amounts for their separate lawsuit.  

DrugNews works only with lawyers that have handled tens of thousands of defective drug and medical device injury cases and are integrally involved with MDL litigation and courts.

Choosing a Cartiva Recall Lawyer

If you or a loved one have suffered complications or repeat surgery due to failure of a Cartiva toe implant, it’s important to have your case examined by a legal expert to see if you have the right to recover damages.  

Our qualified medical device injury lawyers will fully investigate your case, reviewing medical records, safety warnings, recalls and recent studies that your doctor may not normally discuss.  

Most states allow you several years to file a lawsuit after you suffer an injury or discover it may be linked to a dangerous product. However, you should begin the process as early as possible to make sure your lawyer has time to get necessary records and prepare your case.   

DrugNews works only with attorneys and law firms that have successfully handled tens of thousands of lawsuits involving injury or death from drugs and medical devices. And, you can speak directly with a lawyer or patient advocate today, so you’ll be able to decide if you want to proceed.   

We make it easy to get help, find out if you qualify, and quickly file a claim. Our service is offered at no cost to you, and you won’t pay anything to your attorney unless you receive an award. Also, our qualified lawyers can handle most aspects of your case without you ever having to leave your home.   

For more information, or to learn about your options - call, chat or email us today.

Free Case Review

Our attorneys specialize in medical device litigation. "The free evaluation is always confidential."

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