Our lawyers are handling Paragard IUD removal lawsuits in all 50 states. These lawsuits allege the Paragard intrauterine device breaks upon removal because it is made with inflexible plastic and degrades before the device expires. Over 2,500 lawsuits have been lodged against Teva Pharmaceutical and CooperSurgical by women who encountered issues such as breakage during removal or implantation or other complications associated with the Paragard birth control device.
This page provides an update on the Paragard class action lawsuit and speculates on the Paragard settlement amounts.
You can reach our lawyers at 800-553-8082 or get a free online consultation. You pay nothing unless you get a recovery for the injuries related to your Paragard breaking during removal.
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Paragard Class Action Lawsuit
Over one thousand women have filed a Paragard IUD lawsuit claiming that they were injured when a design defect in the popular IUD caused it to fracture during removal and leave foreign objects inside their bodies.
The Paragard lawsuits in the federal courts have been consolidated into an MDL in the Northern District of Georgia. The crux of the class action Paragard suit is that the device is prone to break inside a woman’s body because the IUD is not sufficiently flexible.
In this post, we give a 2025 Paragard lawsuit update. Our lawyers also speculate on how much a Paragard lawsuit might be worth if the litigation is resolved in a global settlement with the manufacturers. When could there be a settlement? Soon. These cases could potentially be resolved in 2025 before the end of the year, with victims getting paid in 2025 if the settlement happens quickly enough. Is that the most likely scenario? We are cautiously optimistic, as they say.
Paragard Class Action Lawsuit Updates 2025
The Paragard IUD litigation is moving forward, and the news continues to favor plaintiffs. With nearly 3,000 cases pending, the momentum is shifting toward accountability. While the manufacturers have fought hard to dismiss claims, judges have allowed key arguments to stand, and bellwether trials are now on the horizon. This is not the kind of litigation that quietly disappears—it is building toward a settlement resolution.
The reality is that Paragard lawsuits have exposed serious design flaws and a failure to warn that put thousands of women at risk. Despite the defense’s efforts to delay, dismiss, and minimize liability, the legal process is advancing. More cases are being filed, critical discovery is underway, and early trial results could put real pressure on the defendants to settle. The longer this goes on, the clearer it becomes that Teva and CooperSurgical will have to answer for the damage their product has caused.
Below, we provide ongoing updates on new case filings, rulings on key legal issues, and where settlement discussions stand. If you are considering filing a claim, now is the time to act. The window for compensation may not stay open forever.
30(b)6 Depositions to Move Forward
March 14, 2025: The judge in the Paragard litigation has ruled on a dispute over 30(b)(6) depositions, which are sworn testimony given by corporate representatives on behalf of a company. Defendants wanted to block these depositions entirely, but the court denied that request, meaning plaintiffs can proceed with questioning company representatives. However, the judge will still consider some of the defense’s concerns about the scope of these depositions.
28 New Cases Added to Paragard MDL as Litigation Expands
March 8, 2025: The Paragard class action MDL has grown by 28 new cases over the last 30 days, bringing the total number of pending cases to 2,965. This steady increase highlights the ongoing legal battle surrounding the Paragard IUD, as more plaintiffs come forward with claims of device breakage and related injuries.
Paragard Trial Dates Pushed Back Amid Revised Scheduling
February 19, 2025: The first Paragard lawsuit in the MDL has been delayed by over a year, with the MDL judge issuing a fourth amended scheduling order. The first bellwether trial is now set for January 12, 2026, followed by additional trials on March 3, 2026, and May 11, 2026. The order outlines detailed procedures for discovery, expert testimony, and depositions of key witnesses, including plaintiffs, healthcare providers, and sales representatives.
Dozens of Paragard Lawsuits Dismissed Due to Statute of Limitations
February 19, 2025: In a ruling favoring Teva Pharmaceuticals and CooperSurgical, Judge May dismissed numerous Paragard lawsuits from plaintiffs in multiple states, citing statutes of limitations. The judge determined that the injury clock started when the IUD broke, even if the full extent of harm—such as infertility or chronic pain—was not immediately apparent. This decision has narrowed the MDL but leaves active cases within the applicable statute of limitations.
Inadequate Warning Labels at the Heart of Paragard Litigation
February 11, 2025: A central issue in the Paragard litigation is the device’s warning label, which plaintiffs argue fails to adequately convey the severity of risks. While the FDA mandated a warning about breakage during removal in 2019, the label remains vague, omitting details about potential complications like organ damage, chronic pain, and infertility. Plaintiffs contend that stronger warnings could have influenced patient and doctor decisions, a key argument in upcoming bellwether trials.
55 New Cases Added to Paragard MDL Amid Settlement Rumors
February 5, 2025: With settlement discussions on the horizon, 55 new cases were added to the Paragard MDL in January, bringing the total number of pending cases to 2,937. Attorneys are prioritizing filing new lawsuits to ensure their clients are eligible for potential compensation, though the timing of filing may not significantly impact settlement amounts.
New Paragard Lawsuit Highlights Long-Term Injuries
February 1, 2025: A California woman has filed a new lawsuit in the Paragard MDL, alleging that her IUD, placed in 2016, broke during removal in 2024, requiring additional surgery. She claims loss of reproductive health, pain, and suffering, underscoring the long-term consequences of device failure.
Settlement Payouts to Reflect Severity of Injuries
January 28, 2025: As settlement discussions progress, the severity of injuries will play a critical role in determining payout amounts. Cases involving emergency surgeries, chronic pain, or infertility are expected to receive higher compensation compared to those with minor complications. The litigation process involves a complex evaluation of medical expenses, lost wages, and emotional distress.
Paragard Warning Label Criticized for Vagueness
January 21, 2025: The Paragard IUD’s warning label, updated in 2019, acknowledges the risk of breakage during removal but fails to detail the potential for severe complications like organ damage or infertility. Plaintiffs argue that the label’s vague language downplays the risks, leaving patients and doctors inadequately informed.
Teva Seeks to Dismiss Cases Ahead of Potential Settlement
January 14, 2025: Teva Pharmaceuticals is actively seeking to reduce the number of pending Paragard cases through procedural dismissals. By identifying documentation deficiencies and enforcing strict procedural standards, Teva aims to narrow the pool of claimants ahead of potential settlement negotiations.
Mediator Appointed to Facilitate Paragard Settlement Talks
January 13, 2025: Retired Judge M. Gino Brogdon Sr. has been appointed as a mediator to oversee Paragard settlement negotiations. This move signals the court’s push for a fair and efficient resolution, with hopes that a global settlement can be reached before the first bellwether trial.
20 New Cases Added to Paragard MDL in December
January 3, 2025: The Paragard MDL saw 20 new cases added in December, bringing the total number of pending cases to 2,882. As the litigation matures, the rate of new case filings has slowed, reflecting the advanced stage of the legal proceedings.
Get More Paragard IUD Lawsuit Updates
December 10, 2024: Discovery Battle Over Contention Interrogatories
Defendants had requested an extension of time to answer contention interrogatories, arguing that their responses should be delayed until the pretrial conference. Plaintiffs opposed the extension, citing the active state of discovery and the need for timely information to prepare their case.
The MDL judge sided with the defendants in granting an extension but stopped short of permitting a delay until the pretrial conference. Instead, the court has stayed defendants’ obligation to respond and stated it would revisit the matter at the next discovery conference.
November 4, 2024: Trial Set for December 1, 2025
The MDL judge has scheduled the first copper IUD bellwether trial for December 1, 2025, and the second for February 2, 2026, pending “confirmation of availability from Defendants’ trial counsel.”
October 23, 2024: FDA Reportedly Look at Paragard IUD Label
The FDA is reportedly reviewing stricter labeling for intrauterine devices, including Paragard, following ongoing reports of breakage complications during removal. This regulatory scrutiny, prompted by nearly 40,000 adverse events reported in the last decade and this litigation, could push manufacturers toward giving a much needed stronger warning and design modifications to make these products safer during removal.
It would not be a shock to see a new warning timed around a global Paragard settlement.
October 21, 2024: Effort to Bring in Teva International Fails
We talked in our September 2 update about plaintiffs’ effort to bring in the parent Teva Pharmaceuticals that is based in Israel into the litigation. That effort failed.
Judge May denied Plaintiffs’ motion to amend their master complaint. The motion sought to add Teva Pharmaceutical Industries Ltd., as a defendant alongside the U.S.-based Teva entities and CooperSurgical.
The judge ruled that the plaintiffs failed to demonstrate the required diligence in filing the motion. The court pointed out that the plaintiffs had been considering adding Teva Ltd. as a defendant since early 2021, yet only filed the motion in mid-2024. The delay, combined with the fact that the plaintiffs had access to the necessary information long before the motion was filed, led the court to conclude that good cause to amend had not been shown. The judge’s order also points out the risk of slowing down the litigation by adding a new defendant at this stage of the game.
The judge is right that this was an unforced error. Always name more defendants rather than less is the rule. You can dismiss them later. But this is not a big deal in the scheme of things.
October 20, 2024: Stories of Women and Paragard Complications
This is a good article for women who are among many who share a common story.
October 11, 2024: Paragard Defendant to $450 Million to Settle Medicare Fraud
Teva Pharmaceutical Industries Ltd. has agreed to pay $450 million to settle allegations that it used charitable organizations to cover Medicare patients’ out-of-pocket costs as a way to pay kickbacks and increase sales of its multiple sclerosis drug, Copaxone. This settlement includes $425 million to resolve a lawsuit filed in Boston in 2020 as part of a broader investigation into drugmakers’ financial support of patient assistance charities. Additionally, the settlement resolves claims that Teva conspired to fix prices for generic drugs.
Maybe we can all agree that the allegations that Teva put profits over women’s best interest in the Paragard litigation are pretty plausible.
October 6, 2024: New Lawsuits in October
We talked in the last update about the litigation slowing down in terms of newly filed cases. Then 12 cases were filed in the first two days of October.
One of those lawsuits was on behalf of a Texas resident who has a story that will sound familiar. Her Paragard device, which was placed in Idaho in 2019 and later removed in Texas in 2022, broke during the removal procedure. As a result, she experienced device breakage and embedment, necessitating additional attempts to remove the remaining fragments. The complaint alleges that the defendants failed to adequately test the product, misrepresented its safety, and concealed information regarding the risks of breakage.
September 19, 2024: New Video on Paragard Litigation
We have a new video providing the latest news and updates on the Paragard lawsuits.
September 13, 2024: Statute of Limitations Dismissal
Teva contends that 236 lawsuits within the Paragard MDL are undeniably time-barred and should be dismissed.
The allegedly untimely cases fall into three main categories:
- Lawsuits where the statute of limitations starts on the date of the Paragard removal surgery.
- Cases blocked by the statute of repose, which prohibits claims after a specific period from the product’s sale or use.
- Claims where strict liability is barred by state law.
Defendants’ problem is that there are fraudulent concealment claims that should make the statute of limitations a matter for the jury. Even if these cases are dismissed—which is probably unlikely—they may still hold some settlement value because Teva/Cooper will not want to deal with an appeal at that point. Still, dismissal would likely reduce the settlement payout of these claims.
The good news is that if you are not one of these 236 plaintiffs? Teva’s strategy seems aimed at clearing these cases before a broader Paragard settlement. My take, and it is just my take, is that a Paragard settlement is likely near and everyone is trying to tie up loose ends before a settlement.
September 6, 2024: New Paragard Lawsuit
A Missouri woman has filed a new lawsuit Wednesday against Teva and Cooper in connection with injuries sustained from the use of the Paragard intrauterine device.
The plaintiff alleges – as every plaintiff in the MDL does – that the Paragard device broke during removal, causing injuries that include pain, suffering, mental anguish, and potential need for further surgeries. The lawsuit alleges counts of strict liability, negligence, breach of warranty, violation of consumer protection laws, and fraud. The plaintiff demands a jury trial and reserves the right to allege further complications or injuries.
September 2, 2024: Push Back on Adding Teva
Plaintiffs filed a motion for Leave to Amend the Second Amended Master Personal Injury Complaint to include Teva Pharmaceutical Industries Ltd. as a named defendant.
Like everything else, Teva is pushing back, claiming that Plaintiffs have not demonstrated the necessary diligence required for such an amendment.
The problem for the defendants is no prejudice in adding another Teva defendant. There is no statute of limitations argument specific to this defendant. Moreover, in the real world, plaintiffs gain a better understanding of who should be the proper defendants and Teva Ltd.’s role in the issues central to the MDL has become more apparent now that new documents have been produced.
August 27, 2024: Defendants Push Back on Motion to Compel
Defendants have filed a response opposing the plaintiffs’ motion to compel the production of custodial files. The plaintiffs argue, as we discuss in the last update, that the defendants have failed to identify relevant custodians and produce their files, despite a previous court order.
The defendants counter that the court never required ongoing identification of custodians and that the responsibility to request specific custodial files lies with the plaintiffs. They further argue that the plaintiffs have not provided a justifiable reason for requesting additional custodial files at this stage, making the request unduly burdensome and disproportionate.
The defendants also contend that they have acted in good faith by providing an updated list of custodians and have met deadlines for producing custodial files. They emphasize that the plaintiffs’ motion lacks a credible basis, as the plaintiffs have been aware of the custodians in question for years and have not previously requested their files. Defendants request that the court deny the plaintiffs’ motion, asserting that the plaintiffs’ request for all 31 custodial files is excessive and unsupported by the facts of the case.
Excessive how? Defendants argue that the production of all 31 custodial files is excessive but they have not convincingly demonstrated how this request would be unduly burdensome, especially in light of the potential relevance of these documents to the case.
August 21, 2024: Custodians Finally Revealed Two Years After Court Order Required Their Identification
Plaintiffs have filed a motion to compel the defendants to produce custodial files for 31 newly identified custodians who were revealed almost two years – two years! – after a court order required their identification.
This motion argues that the defendants delayed disclosing these custodians, thus hindering the plaintiffs’ ability to request and review pertinent custodial files as part of the discovery process. The plaintiffs contend that this delay has caused significant prejudice to their case, as the late disclosure has compressed their discovery timeline and limited their ability to conduct thorough investigations. They request the court to order the defendants to produce these files expediently and at the defendants’ expense to rectify the ongoing prejudice.
The back story is that there are new lawyers representing the defendants, Teva and Cooper, who were formally appointed in September 2023 and February 2024, respectively. According to the motion, the previous attorneys for the defendants had failed to meet their obligations under the custodial file protocol by not timely identifying relevant custodians and producing the required custodial files. The new counsel, upon taking over, threw the old lawyers under the bus and acknowledged deficiencies in the previous productions and undertook additional efforts such as re-interviewing custodians and gathering more documents, which led to the identification of 31 new custodians with potentially relevant information.
August 13, 2024: Defense Lawyers File Motion To Dismiss Many Cases Based On SOL
The defendants have filed motions to dismiss many of these cases, arguing that they are barred by statutes of limitations or statutes of repose. While few cases are expected to be dismissed due to the statute of limitations, the statute of repose could pose an issue for some older cases in certain jurisdictions. A statute of repose sets a final deadline for filing claims, regardless of when the injury was discovered, which could lead to the dismissal of older claims.
This legal strategy foreshadows a potential settlement. Defendants want to get dismissed as many cases as possible through pretrial motions before entering settlement negotiations. By filing these motions, Teva and Cooper aim to reduce the number of active cases, limiting their liability and making the average settlement per case a more attractive number.
August 9, 2024: New Lawsuit Filed Directly In Paragard MDL
Another new copper IUD lawsuit was filed directly in the Paragard class action MDL using the short form complaint earlier this week. The plaintiff in this case originally had her Paragard IUD implanted in Georgia in 2017. Four years later when she had it removed at a Planned Parenthood clinic in New York, the IUD fractured. The fracture left pieces inside of her, causing pain and requiring her to undergo further medical treatments.
July 10, 2024: Southern California Woman Joins Paragard MDL
A woman from southern California became the latest plaintiff to join the Paragard class action MDL. According to the short form complaint filed directly in the MDL, the woman attempted to have her Paragard IUD removed in July 2022. The IUD fractured during removal and she underwent a second procedure in October 2022 in an effort to retrieve the fractured pieces from inside her.
June 29, 2024: State Law in The MDL
Even though multidistrict litigation is a national process designed to streamline complex cases involving many plaintiffs across different states, the laws applied to these cases are state laws, which can vary significantly. This presents a challenge in determining which state’s laws should govern each case within the MDL.
In the Paragard IUD MDL, specific guidelines were issued by the MDL judge to address this issue: For cases transferred from another federal district court under 28 U.S.C. § 1407, the state choice-of-law rules from the transferor court (the court where the case was initially filed) will apply unless the case was filed in an improper venue or jurisdiction. If the venue or jurisdiction was improper, defendants can challenge the application of those state rules.
For cases filed directly in the MDL, the state choice-of-law rules from the district and division identified in the Short Form Complaint will apply, provided the identified court has proper venue and jurisdiction; otherwise, defendants may challenge these rules.
Plaintiffs cannot alter the applicable choice of law by amending the venue in their complaints post-filing, except within a specific timeframe and with consent or court approval. Additionally, no motions to resolve choice-of-law issues can be filed until after the initial bellwether trials unless the applicable law is undisputed. Any changes to the court-set deadlines require court approval for good cause. This structured approach ensures that the diverse state laws are applied fairly and consistently in the consolidated MDL cases.
The law that is applied to the case can be a big deal. One of the most significant differences lies in the treatment of punitive damages, which are awarded to punish defendants for particularly egregious behavior and to deter similar conduct in the future, especially when it comes to punitive damages. Some states have caps on punitive damages or require a higher standard of proof to award them, while others do not have such limitations, potentially leading to significantly higher awards. These discrepancies can greatly affect the strategies of both plaintiffs and defendants, the potential compensation available.
One battlefield in mass tort cases is what law applies to cases in the MDL. The issue is how the choice-of-law analysis should be applied uniformly across the Paragard MDL-2974, which is crucial for determining which state laws govern the cases. Plaintiffs seek flexibility in determining the applicable law for each case individually; defendants advocate for a uniform approach.
Defendants argue that Plaintiffs are attempting to manipulate the choice-of-law process to their advantage without providing any solid legal basis for their position. Defendants maintain that the choice-of-law analysis is a purely legal issue that should be resolved on an MDL-wide basis to ensure consistency and fairness. They emphasize that resolving this legal question now will provide clarity and prevent delays in the litigation process.
In contrast, Plaintiffs argue that the choice-of-law issues are too individualized to be resolved collectively. They cite the need for case-specific determinations despite the defendants’ assertion that such an approach leads to unnecessary complications and delays.
May 6, 2024: Paragard Lawyers Dispute Issues Surrounding ESI Protocol and TAR
Paragard lawyers are disputing the interpretation and application of the ESI Protocol concerning its Technology Assisted Review (TAR) systems and its implications on document production transparency and timeliness.
Plaintiffs’ lawyers are frustrated. They feel left out of critical decisions and question the sufficiency and integrity of the document review process because of the defendants’ alleged unilateral modifications to TAR.
Specifically, the complaint is that this unilateral action violated the agreed-upon ESI protocol, which mandates that both parties meet and confer about the TAR methodology and workflow before its implementation. The plaintiffs were informed only during a document summit in February 2024 about the retraining of TAR despite the process being in motion for several months.
The defense lawyers argue that they have adhered to the necessary protocols and that the plaintiffs’ requests for further involvement and transparency are excessive and unfounded.
Judge May will decide whether the plaintiffs’ concerns justify a deeper inquiry into the defendants’ document production methodologies.
April 3, 2024: Spotlight Investigative Report Alleges That CooperSurgical Ignored FDA Warning
A recent investigative report from Spotlight on America revealed that the FDA had told the maker of the Paragard IUD, CooperSurgical, that it had concerns about the potential for the IUD to break during removal, but CooperSurgical did nothing about it. The FDA concerns were submitted to CooperSurgical following an FDA inspection of one of its Paragard IUD manufacturing facilities. The company appears to have completely ignored this warning from the FDA.
March 21, 2024: Louisiana Woman Files Directly In Paragard MDL
A Baton Rouge, Louisiana woman filed a Paragard lawsuit in the MDL yesterday alleging strict liability and negligence counts. She claims she suffered extensively, including enduring severe pain and the need for complex medical procedures to remove a fractured Paragard device. She says she has loss of reproductive health, permanent physical or cosmetic damage, and emotional distress.
March 8, 2024: Court Makes Several Decisions During Monthly Status Conference
During its monthly status conference last week the court made several decisions, but nothing particularly interesting. It granted permission for counsel representing the Cooper defendants to file a motion to withdraw while Teva’s counsel will step in for the Cooper defendants.
Additionally, the defendants will present a motion to modify the Cooper leadership. Both parties will coordinate to schedule hearings regarding Plaintiffs’ letter briefs and an expected discovery motion. Letter briefs are concise written submissions typically exchanged between parties or submitted to the court to address specific legal issues, procedural matters, or requests for rulings without the need for a formal motion or hearing.
January 22, 2024: New Paragard Lawsuit Filed Friday
A new Paragard copper IUD lawsuit was filed on Friday. A Texas woman alleges injury from breakage when her OB/GYN attempted to remove the device in 2016.
How does she circumvent the statute of limitations? Her complaint alleges tolling/fraudulent concealment. Under this legal principle, the statute of limitations for filing a Paragard lawsuit is paused (or tolled) due to a defendant’s intentional hiding of their wrongdoing.
In such cases, the time limit to bring legal action does not begin until the plaintiff discovers or should have reasonably discovered the fraud or deceit. This principle ensures that plaintiffs have a fair opportunity to seek justice even when defendants have deliberately concealed their harmful actions.
January 2, 2024: Schedule Set For First Paragard IUD Lawsuit Trial
Judge May set out the schedule for the first Paragard IUD lawsuit to trial. This order sets forth various deadlines for case-specific activities, including discovery, expert disclosures, and motions:
Bellwether Trial Schedule: Key Deadlines
Event | Date |
---|---|
Close of case-specific fact discovery and general corporate discovery | April 9, 2024 |
Plaintiffs’ Rule 26 expert disclosure and reports | April 29, 2024 |
Defendants’ Rule 26 expert disclosure and reports | May 27, 2024 |
Deadline for rebuttal experts under Rule 26(a)(2)(D)(ii) | June 18, 2024 |
Close of expert discovery in first Bellwether/trial pool cases | June 9, 2024 |
Daubert Motion deadline in Bellwether trial eligible cases | July 23, 2024 |
Responses to Daubert motions | August 13, 2024 |
Replies to Daubert motions | August 27, 2024 |
Dispositive motion deadline in Bellwether trial eligible cases | September 10, 2024 |
Responses to dispositive motions | October 1, 2024 |
Replies to dispositive motions | October 15, 2024 |
Consolidated pretrial order deadline | November 15, 2024 |
Motion in limine deadline | November 22, 2024 |
Responses to motions in limine | November 29, 2024 |
Pretrial Conference | TBD |
Final Pretrial Conference | TBD |
First Bellwether Trial | TBD |
October 31, 2023: Judge Responds To Unsubmitted Plaintiff Fact Sheet
Plaintiffs in this litigation must fill out a Plaintiff Fact Sheet (PFS) without biographical information and facts about their Paragard lawsuit. However, some did not turn theirs in on time. So, the MDL judge basically said, “Hey, if you didn’t do this, you need to tell us why, or we might drop your case.”
There are six categories for deficient plaintiffs who failed to file a PFS properly:
- Category 1: People who didn’t give a reason for missing the deadline.
- Category 2: People who agree their cases should be dropped.
- Category 3: People who messed up their forms and won’t fix them.
- Category 4: Cases where the lawyers can’t find the person anymore and admit the forms weren’t done right. The judge said their cases are officially dropped for these four categories and cannot be brought back.
- Category 5: People who need more time to finish their forms. They had 21 days from the court’s order on October 5th to turn them in. If they don’t, their cases will be dropped too.
- Category 6: People who turned in their forms late but after the Court’s warning. Their forms are accepted, and they’re good to go.
This is generally a good development. Getting rid of Paragard IUD lawsuits that are now really lawsuits allows everyone to move forward on the real cases that matter.
October 2, 2023: Paragard MDL To Focus On Factual Discovery For Bellwether Candidate Pool Cases
As set forth in the recent Case Management Order, the focus in the Paragard MDL for the next few months will be case-specific factual discovery in the bellwether candidate pool cases. Depositions of the plaintiffs in these cases will take place over the course of this month. The purpose of this discovery phase is to give the parties more information about bellwether pool cases so they can assess their strengths and weakness.
June 30, 2023: CMO Requires All Plaintiffs To Submit Plaintiff Fact Sheet
The Court’s PFS CMOs required all plaintiffs involved in MDL No. 2974 to submit a completed Plaintiff Fact Sheet (PFS) and signed authorizations to the Defendants by November 4, 2022. So… long ago. There are always mass tort plaintiffs who bring claims that either do not have viable claims or simply decide not to pursue a lawsuit. In this case, 132 Paragard plaintiffs are in that boat.
The deadline to submit the required information or provide an explanation for not doing so has passed, and the MDL judge will likely dismiss those claims. This allows a greater focus on those with serious cases, which may pave the way for a future global settlement.
June 19, 2023: Paragard MDL Continues To Move Slow
This litigation is moving slowly. But the statute of limitations is an issue if you are looking to file a Paragard lawsuit. The message: if you have a claim, call a Paragard lawyer—us, whoever—now.
June 2, 2023: Initial Bellwether Discovery Pool Close To Finalization
The initial pool of Paragard bellwether discovery cases is close to being finalized. Over the next few weeks, these cases will go through an accelerated fact discovery phase involving depositions of the plaintiffs and other fact witnesses. The information obtained from this discovery phase will then be used to narrow down the pool to six cases.
May 1, 2023: Judge May Expresses Optimism Towards Possible Settlement
At a recent court conference, Judge May closed a hearing expressing optimism that the Paragard settlement mediator, Gino Brogdon Sr., will be able to push settlement talks forward and encouraged the parties to get moving toward that end. This makes us optimistic, but that optimism is chilled by how far away the first trial is. Because trial dates put on the pressure that leads defendants to offer reasonable settlement amounts.
April 18, 2023: 64 New Cases Added To MDL
In the Paragard class action MDL, 64 new cases were added, propelling the total number of plaintiffs to 1,780. The ongoing trend portends the prospect of crossing the 2,000 mark before the year’s end. Bellwether trials, frustratingly, remain 18 months away.
March 15, 2023: 34 New Cases Added To MDL
Thirty-four new plaintiffs with pending cases were added to the Paragard class action MDL over the last 30 days. Last month, the MDL posted its second-highest monthly volume ever with 105 new cases, so this is a sharp drop-off. The total number of pending Paragard IUD lawsuits in the MDL is 1,716.
February 25, 2023 Update: Judge Establishes Procedure For Selecting Bellwether Test Trial Representatives
The presiding judge in the federal Paragard IUD lawsuits has established a procedure for selecting a group of 10 representative cases for the initial bellwether trials slated for 2024. Fifteen cases will be nominated by the plaintiffs for the bellwether pool, which will then be reduced to ten through a process of eliminations and challenges from both parties. These ten cases will undergo detailed, case-specific discovery, with three ultimately chosen to proceed in the initial bellwether trials starting in Georgia in March 2024.
What is a bellwether trial? A bellwether trial is a legal process employed in mass tort litigation to gauge how juries might respond to the evidence and testimonies that are expected to recur across many similar cases. This approach involves preparing a small, representative set of cases for early trial dates. The outcomes of these trials are used to guide decisions in future trials and potential settlements.
February 5, 2023: Bellwether Process Remains A Work In Progress
The bellwether process in the Paragard MDL remains a work in progress 25 months after the MDL class action was established. A status conference was held before Judge May this week. Still, instead of finalizing the bellwether process, she simply offered “guidance” to the parties on their competing proposals for how the bellwether program should be handled. In the meantime, corporate depositions are getting underway for the primary defendants, Cooper Surgical and Teva Pharmaceuticals.
January 25, 2023: Judge M. Gino Brogdon Sr. Appointed As Settlement Mediator
Looking for some good news in the Paragard litigation? A retired Fulton County, Georgia judge, M. Gino Brogdon Sr., was appointed by the Paragard class action judge to serve as a settlement mediator.
We don’t think Teva and Cooper Surgical are on the phone with this mediator right now trying to set up settlement talks. A trial is too far away for the defendants to feel any urgency to settle these lawsuits. Brogdon’s appointment was made by the Court and not at the parties’ request, so this is not a sign that a settlement might be in the works already. That said, any direction in the settlement path for victims who have already waited too long for compensation is good.
January 9, 2023: 934 Adverse Incident Reports Involving Paragard IUD Fracture Reported To FDA In 2022
934 adverse incident reports involving fracture of the Paragard IUD during removal were reported to the FDA Adverse Event Report Database in 2022. This is three times the number of events reported for the Paragard just two years ago, and it suggests that we could see continued growth in the number of Paragard product liability cases in the MDL in 2023. It also shows—importantly—that Paragard removal breakage is more common than the defendants claim.
Frequently Asked Questions About the Paragard IUD Lawsuit
Who qualifies to file a Paragard IUD lawsuit?
What is the status of the Paragard MDL lawsuit?
What is the potential settlement amount for a Paragard IUD lawsuit?
While no official Paragard IUD lawsuit settlement amounts have been announced, historical settlements in defective medical device lawsuits provide insight into what plaintiffs might expect. Based on similar mass tort cases, estimated Paragard IUD settlement payouts could fall within these ranges:
- Severe cases (hysterectomy, infertility, major surgery): $100,000 – $380,000
- Moderate cases (multiple procedures, chronic pain, partial removal): $40,000 – $75,000
- Mild cases (fragment removal without major complications): $10,000 – $30,000
A Paragard compensation claim will likely be evaluated based on the severity of injuries, medical expenses, and the long-term impact on reproductive health.
We give more background to our thinking on Paragard settlement amounts below.
What are the main allegations in the Paragard litigation?
The Paragard copper IUD lawsuits allege that:
- The Paragard IUD is defective, prone to breakage during removal, and unsafe for long-term use despite being marketed as a 10-year birth control device.
- Teva Pharmaceuticals and CooperSurgical failed to warn patients about the risks, misleading doctors and consumers about the device’s propensity to fracture.
- The manufacturers concealed safety concerns despite thousands of adverse event reports and an FDA warning about copper IUD breakage.
- Women suffered perforated uteruses, chronic pain, infections, and permanent infertility due to broken Paragard fragments that migrated into surrounding organs.
The Paragard litigation is centered on claims of product liability, failure to warn, and negligence.
What should I do if my Paragard IUD broke during removal?
What is the deadline to file a Paragard lawsuit?
The Paragard lawsuit statute of limitations varies by state, but most product liability claims must be filed within two to four years from the date of injury or the date you discovered the injury. Some states apply the discovery rule, allowing lawsuits to proceed if plaintiffs only recently became aware of the extent of their injuries.
However, recent court rulings in 2025 have dismissed cases based on strict statute of limitations interpretations. In some states, the judge ruled that the clock starts the moment the IUD breaks—even if a woman did not experience immediate complications. This has led to dismissals in certain states where plaintiffs were unaware of their injuries until years later.
If you are considering filing a Paragard IUD lawsuit in 2024 or 2025, it is crucial to contact a lawyer immediately to ensure you do not miss your filing deadline.
Is there a Paragard class action lawsuit?
Has there been a Paragard IUD recall?
How much does it cost to hire a lawyer for a Paragard lawsuit?
What should I do if I believe I have a Paragard claim?
If your Paragard IUD broke during removal, caused pain, infertility, or required additional surgery, you may be entitled to significant compensation. The best way to protect your rights is to contact a Paragard lawyer immediately.
To discuss your case with an attorney, call 800-553-8082 for a free consultation or fill out an online form. Your time to file a Paragard IUD lawsuit may be limited.
Paragard Lawsuits
The Paragard is a type of birth control known as an intrauterine device (IUD). The Paragard is a Y-shaped device about the size of a quarter with a copper coil around the center. It has a plastic frame made of polyethylene and barium sulfate. Paragard, the only hormone-free IUD in the U.S., and controls 17% of the U.S. IUD market in 2024.
The IUD is placed at the base of the uterus by a doctor, and it remains there for as long as ten years, providing continuous protection against pregnancy. The Paragard was designed to be easily removed by pulling on a removal cord at the doctor’s office.
Unfortunately, the Paragard copper IUD design has a hidden defect that has led to problems during the removal process for many women. The plastic arms at the base of the Paragard are supposed to flex upwards when the device is pulled out for removal. In many cases, however, the plastic arms become rigid and break off inside the patient during removal. This results in sharp pieces of plastic inside the woman’s uterus.
Accordingly, the plaintiffs in the Paragard class action lawsuit are all women with a Paragard implant that later broke while still in their bodies. The IUD breaks because the flawed design does not provide sufficient flexibility. Specifically, Paragard lawsuits allege that Paragard raw plastic T units failed to meet the minimum flexibility requirements with the IUD’s approved expiration date (i.e., shelf life) before installing the copper sleeves. So the arms become more rigid over time, and these devices are marketed as a long-term solution.
Failure to Warn of Paragard Complications
There is also a failure to warn component to the Paragard class action lawsuit. Plaintiffs claim the defendants knew Paragard could cause serious harm to women due to its propensity to break in utero or during removal but failed to adequately warn doctors and patients of the risk. No one is arguing for a Paragard recall. Just warn doctors and women of what you know about the dangers.
The defendants in the Paragard lawsuits, including Teva Pharmaceuticals and CooperSurgical, could have been aware of the risks associated with the device breaking during removal based on numerous reports filed between 2009 and 2021. During this time, over 2,000 incidents of Paragard breakage were reported, indicating a recurring problem. Despite these reports, the information did not translate into enhanced warnings for doctors or patients. This failure to act raises significant concerns, as plaintiffs argue that the companies had ample opportunity to update the product’s labeling or issue stronger safety warnings to prevent harm.
Instead, the manufacturers continued to market Paragard without adequately disclosing the risks associated with the device’s fragility, particularly during removal. Breakage of the Paragard device can lead to severe complications, such as pieces of the IUD becoming embedded in the uterus, necessitating surgical interventions. The plaintiffs argue that had the risks been made clear, many women might have opted for alternative birth control methods or taken additional precautions during removal procedures.
This lack of transparency about known risks has fueled the litigation. Paragard lawsuits allege the defendants intentionally concealed the severity and frequency of the risks associated with Paragard’s removal. Why? The same reason any medical device company hides the risks of their product: a warning would decrease sales and profits.
Eventually, to cut their losses, the warning label on the Paragard IUD was updated in 2019 to include the risk of breakage during removal. The label now cautions that the device may break, making removal difficult, and that fragments, such as the arms, can become embedded in the uterus. But this warning was either too little or too late for too many women.
Paragard IUD Lawsuits Will Be Resolved in a Global Settlement
The Paragard lawsuits will eventually be resolved with a global settlement. This is how almost all product mass torts are resolved and not dismissed by a judge. The Paragard MDL was formed at the end of 2020 and new Paragard cases continued to get filed and added to the MDL. The MDL judge will oversee a consolidated “group discovery” process between the plaintiffs and defendants. The focus of the discovery process will be on the design flaw in the Paragard and what the defendants knew.
When the process of consolidated discovery in the Paragard MDL is completed, the litigation will move into the bellwether trial phase. This is where jury trials are conducted in a select handful of individual Paragard chosen by the parties. The results of these initial bellwether “test trials” significantly impact the litigation. They usually dictate how quickly the defendants will negotiate a global settlement and how much the settlement payouts will be.
What Will a Global Paragard Settlement Look Like?
The best way to understand how global settlements work in the MDL process is to consider a simplified hypothetical example. Let’s say Acme Company is defending 10,000 lawsuits in an MDL. The class action complaint alleges that its medical device was defective and caused patients to suffer internal organ damage. The class action MDL goes through 18 months of discovery. At the close of discovery, 20 plaintiffs are selected by the parties for bellwether trials. The plaintiffs pick ten, and Acme decides the other 10.
Over the next six months, jury trials are completed in three of these ten cases. The first case results in a $5,000,000 verdict. The second case (one of the defense picks) results in a defense verdict. The third case ends with a $1,200,000 verdict for the plaintiff. Based on these results, Acme decides to settle the remaining 10,000. After six months of negotiation, a global settlement agreement is approved by the MDL judge.
Under the settlement, Acme agrees to pay $1 billion to settle all 10,000 pending cases. If divided evenly, this would result in a payout of $100,000 per plaintiff. But the settlement creates a complicated tiered system. The settlement plan ranks each plaintiff based on the severity of their injuries (and other factors). Plaintiffs in the highest tiers get larger payouts, and those in the lower settlement tiers get smaller payouts.
Estimated Settlement Payout in Paragard Lawsuits
Our lawyers cannot predict with certainty how much the settlement payout in the Paragard lawsuit might be. When there is a trial – which should be in 2025 – we will get a much more focused idea of what Paragard settlement compensation might be. It is not too early, however, to make an educated guess about the potential settlement amounts of the average case in the class action, which might be based on settlement payouts in prior mass tort cases with similar allegations.
Based on global settlements in prior mass tort cases involving defective medical devices and internal damages, we believe that Paragard cases in the highest settlement tier will have a value between $100,000-$380,000. Paragard plaintiffs in the second tier can probably expect payouts between $40,000-$75,000. There will probably be a lower, third tier of plaintiffs who get smaller payouts ranging from $10,000-$30,000.
Settlement Tier Estimated Settlement
Tier I $100,000-$380,000
Tier II $40,000-$75,000
Tier III $10,000-$30,000
What Paragard settlements will have the higher payouts? If a young woman becomes infertile, those will be solid cases, and the likely settlement payout for that victim will likely exceed the high range of this compensation estimate. Indeed, you would expect a successful jury verdict in a Paragard infertility case to be in the millions, particularly for a woman who did not have children before getting the Paragard IUD.
It is impossible to emphasize how speculative these Paragard individual settlement compensation payouts are. Because all these projections make the leap of assuming that a judge will allow the Paragard lawsuits to go to trial. Before these cases ever get to a jury, the MDL judge will have to decide whether there is enough scientific proof that a reasonable jury could accept.
Is this a challenge in the Paragard lawsuits? It is a challenge in most mass tort lawsuits. What your gut and science tell you are often two different things. But our Paragard attorneys believe the science supports the plaintiffs’ claims that the design was defective (and the defendants knew it and did not tell anyone).
Hiring a Paragard Lawyer
Each victim who has filed a Paragard class action lawsuit had a Paragard break while it was still inside her body. If this happened to you, call a Paragard lawyer. You can reach us at 800-553-8082 or get a free online consultation. You pay nothing unless you get a recovery.
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