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— Cartiva toe implant · failure & revision claims

Cartiva Implant Lawsuit: Did Your Toe Implant Fail?

You had the surgery so you could keep moving. The whole point was avoiding a fusion — keeping the joint, keeping your stride, getting back to walking without thinking about it. Then the pain came back. Or it never really left. Maybe a scan showed the implant had sunk into the bone. Maybe you have already had the fusion you were trying to avoid.
Updated July 31, 2026

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— Eligibility

Who May Qualify for a Cartiva Implant Lawsuit

You may qualify for a Cartiva toe implant lawsuit if the points below describe you. These are the guidelines participating law firms use when they review a claim.
You had a Cartiva implant in your big toe
Placed for arthritis at the base of the big toe. If you are not sure of the brand, that is normal — it is in your surgical records and we can help you find it.
The surgery happened between 2016 and 2024
The recall covers every model and size sold from July 2016 through October 2024. If your surgery falls in that window, your device was included.
The pain came back, or never left
The implant was supposed to end the pain and keep the joint moving. Continued or returning pain and stiffness is the most common complaint.
Imaging showed the implant sank, moved or broke
Sinking into the bone is called subsidence and it is the leading reported problem. Loosening, displacement and fragmentation also count.
You needed another operation
Removal, replacement, or a fusion of the joint. A fusion is especially significant, because avoiding one is usually why people chose this implant.
You still have the implant and it hurts
You do not have to have had revision surgery already. If you are living with pain or a doctor has recommended another operation, your situation can still be reviewed.

Meeting these guidelines does not mean you have a valid claim. It means a participating law firm is likely to review it. That firm decides on its own whether to take your case. Some claims are turned down, and some recover nothing. Direct2Attorney cannot judge the legal merits of your case, give legal advice, or file anything for you.

Do not know what brand of implant you got?

Hardly anybody does. It is written in your operative report and the surgery center’s implant log, and a firm can pull those records for you. Not knowing is not a reason to skip the review.

— Educational

What You Need to Know About the Cartiva Implant

Arthritis at the base of the big toe wears away the cartilage until bone grinds on bone. It hurts to push off, to walk uphill, to wear ordinary shoes. For a long time the standard fix was fusion — joining the two bones so the joint cannot move at all. It reliably stops the pain, but the joint is gone for good.

The Cartiva Synthetic Cartilage Implant was sold as the alternative. Approved by the FDA in 2016, it is a small hydrogel plug, about the size of a pencil eraser, pressed into the end of the bone to act like cartilage. The promise was pain relief without giving up the joint. That promise is exactly why most patients chose it.

Lawsuits allege the device did not hold up. The central claim is subsidence — the plug sinking down into the bone. When it sinks, the joint loses its cushion and height, and the pain and stiffness come back. Other claims involve the implant loosening, shifting out of place, or breaking apart.

The lawsuits allege that Cartiva, Wright Medical and Stryker knew failure rates were far higher than what doctors and patients were told, and kept selling the device anyway.

The recall

What was recalled

In October 2024 Stryker recalled the Cartiva Synthetic Cartilage Implant. The FDA posted a Class II recall in December 2024.

  • All models and all sizes
  • Every unit distributed from July 2016 through October 2024
  • Based on post-market data showing higher failure rates than expected

Problems the recall listed

  • Revision surgery
  • Implant removal
  • Subsidence — sinking into the bone
  • Displacement — moving out of position
  • Ongoing pain
  • Nerve damage
  • Fragmentation — breaking apart
A Class II recall means the FDA considers the problem capable of causing temporary or reversible harm, with a remote chance of serious harm. It does not mean every implant will fail. Product and company names are used here only to identify the products and parties at issue. Direct2Attorney is not affiliated with, endorsed by, or sponsored by Cartiva, Inc., Wright Medical Group, Stryker Corporation, the FDA, or any court.

Where the cases actually stand

This litigation is genuinely early
On February 5, 2026 the federal courts centralized Cartiva cases into MDL No. 3172, before Chief Judge Kristine G. Baker in the Eastern District of Arkansas. That is a meaningful step — it means the courts see common issues worth handling together — but be clear about the stage: only about 14 cases were on the federal docket when the MDL was formed, no trial date has been set, and there is no settlement of any kind. The first organizational hearing is scheduled for August 26, 2026 in Little Rock. Anyone describing this as a case that is about to pay out is getting ahead of the record.
Why early can still be worth acting on
The recall covers eight years of implants and every size sold, so the number of people potentially affected is far larger than the number who have filed. Cases are being filed nationwide and firms are actively reviewing them. Being early in a litigation is generally better than being late: records are easier to obtain, your surgeon still remembers you, and state filing deadlines have not started running out. Stryker has also resolved some individual cases privately, though no terms have been made public.
Not every implant failed
Some people did well with this device and still are. A recall does not mean every patient was harmed, and having had a Cartiva implant is not by itself a claim. What matters is whether yours failed and what it cost you. That is what a review looks at.

⚠️ This page is general information, not medical advice

If you have a Cartiva implant and you have ongoing pain, stiffness, swelling, numbness, or you have started changing how you walk to protect the toe, see your foot and ankle surgeon. Imaging can show whether the implant has sunk or moved. Do not delay a medical appointment for a legal one, and do not stop or change treatment based on what you read here.

— Compensation

What Compensation May Cover

If a claim succeeds, compensation is meant to cover what the failed implant has cost you — in money, in work, and in how you move through your day. Here is what these claims typically seek.

Financial losses

  • Cost of the original implant surgery
  • Revision, removal or fusion surgery
  • Imaging, injections and follow-up care
  • Physical therapy and rehabilitation
  • Orthotics, braces and custom footwear
  • Wages lost during recovery
  • Reduced ability to do physical work

Personal losses

  • Pain and physical suffering
  • Permanent loss of joint motion after a fusion
  • Difficulty walking, standing or working
  • Giving up sports, hiking, running or dancing
  • Emotional distress from a failed surgery
  • Loss of enjoyment of everyday life
  • Punitive damages, where a state allows them

What affects the value of a claim

Your medical situation

  • Whether you needed revision surgery
  • Whether you ended up with a fusion
  • How soon after implantation it failed
  • Whether you have permanent limits now

Your case details

  • Whether records confirm the device brand
  • Imaging showing subsidence or displacement
  • Your age, work and how active you were
  • Your state’s filing deadline

No one can tell you what your claim is worth before reviewing your records, and no one can promise you will recover anything at all. There is no settlement in this litigation — no fund, no payment schedule, and no court-approved amounts. Any figure you see quoted online for Cartiva claims is speculation. Any service that quotes you a guaranteed dollar figure is telling you something it cannot know. Past results do not guarantee or predict a similar outcome in any future case. Attorney fees, case costs, and medical liens are taken out of any recovery.

— The process

How It Works: 4 Simple Steps

You do not need to know the brand of your implant or have your records in hand. You just need to answer a few questions and let the people who do this every day take it from there.

STEP 01 01

Tell us what happened

Fill out the short form or call. You tell us roughly when the implant went in, what went wrong, and whether you have had another surgery. It takes about two minutes. There is no cost and no obligation.

STEP 02 02

A law firm reviews your case

If your situation fits, we connect you with a participating law firm. That firm looks at your case on its own and decides whether to represent you. If it does, you sign an agreement directly with the firm.

STEP 03 03

The firm confirms your device

You sign a records authorization. The firm pulls your operative report and the surgery center’s implant log to confirm the brand, gathers your imaging and treatment records, and files your claim.

STEP 04 04

Your claim joins the litigation

Your case moves through MDL 3172 alongside the others. Your firm keeps you updated as the court sets its schedule. You are never required to accept an offer you do not want.

— Why people use us

Trusted Help, at No Upfront Cost

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No upfront fees

The review is free. Participating firms work on contingency, so a fee is owed only out of a recovery. No recovery, no attorney fee.

⚖️

Firms in this MDL

We connect you with firms handling medical device claims — ones already filing into MDL 3172 and following the court’s early schedule.

📄

We help find your device

Not knowing the brand stops most people from calling. Your surgical records have the answer, and a firm can pull them for you.
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Private and secure

Your information is encrypted and handled according to our Privacy Policy. You are never obligated to move forward.

What Direct2Attorney is

A legal marketing and referral service. We check whether your situation matches what participating law firms are looking for, and connect you with one of them if it does.

What Direct2Attorney is not

We are not a law firm. We cannot give you legal advice, represent you, or file anything on your behalf. Only a law firm you sign with can do that.

— Free case review

Get Your Free Case Review

If you had a toe implant between 2016 and 2024 and the pain came back, the implant sank, or you ended up having the fusion you were trying to avoid, find out where you stand. You do not need to know the brand — that is in your records. It takes about two minutes, it costs nothing, and your state’s filing deadline is running whether or not you look into it.

— QUESTIONS

Cartiva Implant Lawsuit FAQs

Who qualifies for a Cartiva implant lawsuit?

Participating law firms are generally reviewing claims from people who had a Cartiva Synthetic Cartilage Implant placed in the big toe between 2016 and 2024 and then had ongoing or returning pain, imaging showing the implant sank or moved, or surgery to remove, replace or fuse the joint. You do not need to have had revision surgery already to have your claim looked at.

How do I know if I had a Cartiva implant?

Most patients do not know the brand of what was put in their foot, and that is normal. The device name is recorded in your operative report and in the implant log at the surgical center or hospital. Your surgeon’s office can also tell you. You can request those records yourself, and a participating law firm can request them for you once you sign an authorization.

Was the Cartiva implant recalled?

Yes. In October 2024 Stryker recalled the Cartiva Synthetic Cartilage Implant, and the FDA posted a Class II recall in December 2024 covering all models and sizes distributed from July 2016 through October 2024. The recall cited a higher than expected rate of revision, removal, the implant sinking into the bone, displacement, pain, nerve damage and fragmentation.

What does subsidence mean?

Subsidence is the word for the implant sinking down into the bone of the big toe joint. It is the most common complaint reported by Cartiva patients. When it happens the joint loses height and cushioning, which can bring back the pain and stiffness the surgery was meant to fix, and it often leads to another operation.

Do I need to have had revision surgery already?

No. Having a revision or a fusion generally makes a claim stronger because it documents the failure, but people who still have the implant and are living with pain, stiffness or imaging that shows a problem can still have their situation reviewed. Talk to your surgeon about your symptoms and have your legal options looked at separately.

How much does a Cartiva implant lawyer cost?

Nothing to ask. The case review is free with no obligation. If a participating law firm takes your case, it will normally work on contingency. That means the fee comes out of a recovery, and no fee is owed if there is no recovery.

Does filling out the form create an attorney-client relationship?

No. Direct2Attorney is a legal marketing and referral service, not a law firm. An attorney-client relationship may form only after a participating law firm reviews your information and signs a separate representation agreement with you.

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— Sources

Where this information comes from

  1. In re: Cartiva Synthetic Cartilage Implant Products Liability Litigation, MDL No. 3172, master docket 4:26-md-03172-KGB, U.S. District Court for the Eastern District of Arkansas, Chief Judge Kristine G. Baker — centralized by the Judicial Panel on Multidistrict Litigation on February 5, 2026.
  2. Judicial Panel on Multidistrict Litigation, pending MDL docket statistics, March 2026.
  3. Court letter setting the initial organizational hearing for August 26, 2026 in Little Rock, with leadership proposals and case status summaries due August 19, 2026.
  4. U.S. Food and Drug Administration Class II recall notice for the Cartiva Synthetic Cartilage Implant, posted December 2024, covering units distributed July 2016 through October 2024.
  5. Stryker recall communication to physicians, October 2024, listing revision, removal, subsidence, displacement, pain, nerve damage and fragmentation.
  6. Plaintiffs’ complaints filed against Cartiva, Inc., Wright Medical Group N.V. and Stryker alleging defective design and failure to warn.

Litigation facts change frequently. This page was last reviewed on July 31, 2026. No bellwether trial date had been set and no settlement existed as of that date. Failure rates described in complaints are allegations that have not been established in court. Nothing here is legal or medical advice.