Paragard Lawsuit in December 2023: Insights, Settlements & What to Know

In the realm of birth control, the Paragard IUD emerged as a preferred non-hormonal method for many women, lauded for its long-term effectiveness and relative ease of use. Yet, in a twist of events, the very device that promised security has become the epicenter of a mounting legal battle. The Paragard lawsuit, now a subject of intense scrutiny, highlights the potential risks and complications associated with this medical device. For potential plaintiffs, victims of Paragard IUD complications, and the wider public, understanding the intricacies of this lawsuit is crucial. This article provides a comprehensive insight into the controversy surrounding the Paragard IUD, detailing the origins of the claims, the side effects experienced by users, and the avenues available for those seeking justice. Whether you're a legal professional, a medical researcher, or someone affected by the device, this guide aims to shed light on the pressing questions surrounding the Paragard lawsuit.

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Paragard Lawsuit Updates and Developments

The Paragard IUD lawsuit has seen numerous developments over the past months. Here's a month-by-month breakdown of the significant milestones:

  1. The Paragard class action Multi-District Litigation (MDL) has recently seen an addition of 37 new cases, bringing the total pending case count to 2,283. Notably, the influx of new cases in the Paragard MDL has slowed down over the last few months, indicating a possible sustained trend in the litigation's progression. Despite this, our firm continues to receive inquiries from potential claimants interested in filing a Paragard lawsuit, although the current rate of new cases is noticeably lower compared to six months ago.

  2. The Paragard class action Multi-District Litigation (MDL) has seen a modest increase this month, with 37 new cases added, bringing the total number of pending cases to 2,283. This trend suggests a potentially enduring shift in the pace of the litigation, indicating a more consistent and steady progression in the handling and filing of new cases associated with the MDL.

  3. In the Paragard MDL (1:20-md-2974), the court mandated completion of a Plaintiff Fact Sheet (PFS) by all involved. However, several participants missed their deadlines. The court, after issuing a warning and requesting explanations, has categorized these non-compliances into six distinct groups:

    1. Cases from categories 1-4, encompassing those who didn't provide a valid reason for non-compliance, failed to correct errors, or were unreachable, have now been officially dismissed.
    2. Category 5 comprises individuals who sought extra time. They've been granted an additional 21 days. Failure to meet this extended deadline will result in their cases being dismissed.
    3. For Category 6, submissions that arrived late but post-court warning have been accepted and will proceed.
  4. The Paragard class action Multi-District Litigation (MDL) saw an influx of 99 additional cases over the past month, elevating the total number of active lawsuits to 2,246. This expansion comes as the legal process continues to gear up for the first bellwether trial, which is set to provide crucial insights but remains a year away on the legal timeline.

  5. The Paragard class action MDL has seen significant growth with the addition of 99 new cases over the past month. This increase elevates the total count of active cases in the litigation to 2,246. This development comes as we stand one year away from the scheduled commencement of the first bellwether test trial, marking a critical juncture in the ongoing litigation.

  6. As the Paragard class action MDL marches towards its first bellwether trial scheduled for next year, case-specific fact discovery takes center stage. The upcoming month is slated for comprehensive depositions involving plaintiffs, their spouses, and other pertinent fact witnesses from the bellwether candidate cases. Following this, the spotlight will pivot to expert witness depositions, setting the stage for critical advancements in this unfolding litigation.

  7. Around 100 cases in the Paragard class action litigation are set to be dismissed due to non-compliance with specific requirements. The majority of these plaintiffs have lost touch with their attorneys, leading to potential dismissals.

  8. The Paragard class action MDL saw an addition of 53 cases, bringing the total to 2,063. This month marked continuous growth in the number of cases added to the MDL.

  9. The Court emphasized the importance of plaintiffs submitting their Plaintiff Fact Sheet (PFS) from a previous mandate in November 2022. Currently, 132 plaintiffs risk case dismissal due to non-compliance. Additionally, 44 new cases were added to the MDL, and an accelerated fact discovery phase is anticipated for the initial pool of Paragard bellwether discovery cases.

  10. There was a significant spike in the number of cases added to the Paragard class action MDL, with 186 new cases introduced. This growth brought the total number of cases to 1,966. A court conference also hinted at optimism regarding advancing Paragard settlement talks.

  11. 64 new cases were added to the class action MDL, with projections suggesting that the total number of plaintiffs could cross 2,000 by the year-end.

  12. The MDL witnessed the addition of 34 new plaintiffs. This was a decrease compared to the previous month, which saw a high of 105 new cases.

  13. The judge provided an outline for selecting representative cases for the first bellwether trials in 2024. A bellwether trial helps gauge jury reactions to repeated testimonies and evidence across multiple cases, guiding future trials and potential settlements. Additionally, 105 new lawsuits were added to the Paragard class action MDL.

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The Origins of the Paragard Controversy

Paragard Lawsuit
Paragard Lawsuit

Paragard, originally hailed as a breakthrough in contraceptive technology, is a copper intrauterine device (IUD) that was introduced to the market after receiving approval from the Food and Drug Administration (FDA) in 1984. Designed as a non-hormonal form of birth control, it stood out in the contraceptive market because it offered a long-term solution without the hormonal side effects commonly associated with other birth control methods.

However, over the years, some cracks began to appear in its reputed safety profile. Reports started surfacing where users alleged that the Paragard IUD had a tendency to fracture or break during the removal process. Not only did these breaks pose an immediate physical risk, but they also led to complications ranging from infections to surgeries to remove the broken pieces.

These alarming reports were not isolated incidents. As more women experienced similar complications, the whispers of discontent grew louder. Medical professionals, initially advocates for the device, began to approach it with caution, given the rising number of reported issues.

Legal scrutiny soon followed. Affected women turned to the judicial system, seeking redress for the pain, suffering, and medical costs they incurred due to the alleged design defects of the Paragard IUD. These claims form the crux of the ongoing Paragard IUD lawsuit, which accuses Teva Pharmaceuticals and Cooper Surgical, the manufacturers and distributors of Paragard, of failing to adequately warn users about the potential risks and of releasing a product with a design defect into the market.

The controversy surrounding Paragard is a classic case of medical innovation clashing with unintended side effects. As the legal battles unfold, the true extent of the Paragard issue and the responsibilities of its manufacturers are yet to be fully understood.

What are Paragard's Side Effects?

Paragard, as a non-hormonal IUD, was designed to minimize many of the side effects commonly associated with hormonal birth control methods. However, as more users shared their experiences and medical reports were published, it became evident that Paragard had its own set of complications.

  • Device Fracturing: The most publicized concern associated with Paragard is the device's tendency to fracture or break upon removal. In many cases, fragments of the device remain inside the body, leading to a slew of complications.
  • Internal Injuries: If the device breaks during removal or migrates from its intended position, it can cause internal injuries. These injuries can range from punctures or perforations of the uterus to damage to nearby organs.
  • Infections: Fragments left behind in the body can act as a nidus for infections. If untreated, these infections can lead to more severe health complications, including pelvic inflammatory disease.
  • Surgeries to Remove Fragments: Often, the broken pieces of the IUD cannot be removed without surgical intervention. These surgeries, apart from being invasive, come with their own set of risks and can be a source of considerable distress and financial burden to the affected individuals.
  • Inflammation and Scarring: In some users, the presence of the copper IUD or its fragments has led to inflammation and scarring in the pelvic region. This can lead to chronic pain and may impact fertility.
  • Ectopic Pregnancies: While rare, there have been reports of ectopic pregnancies in women using Paragard. An ectopic pregnancy, where the fetus develops outside the uterus, is a medical emergency and can be life-threatening.
  • Heavy Menstrual Bleeding and Pain: Some women reported heavier than normal menstrual bleeding and increased menstrual pain after the insertion of Paragard.

It's important to note that while many women use Paragard without experiencing adverse side effects, the number of reported complications is significant enough to merit attention. The combination of these side effects and the associated medical, emotional, and financial costs have been the driving forces behind the Paragard birth control lawsuit.

How Many People are Affected by Paragard Lawsuit?

The Paragard lawsuit has garnered significant attention due to the breadth of its potential impact. As an FDA-approved contraceptive option available since 1984, Paragard has been a choice for millions of women seeking a long-term, non-hormonal birth control method.

However, the exact number of affected individuals can be broken down into several categories:

Reported Incidents: While it's challenging to pinpoint an exact number of complications directly attributable to Paragard, thousands of adverse event reports have been submitted to the FDA concerning the device. These reports range from device fracture to more severe complications like organ perforation.

  1. Legal Claims: As awareness of the potential complications associated with Paragard has grown, so too has the number of legal claims. Hundreds, potentially even thousands, of women have either filed lawsuits or are in the process of doing so, alleging harm from the device.
  2. Potential Future Claims: Given the widespread use of Paragard over several decades, it's plausible that many affected individuals are yet to come forward, either because they haven't connected their complications to the device or are unaware of the ongoing lawsuit. As publicity around the Paragard lawsuit continues to grow, the number of claimants might rise significantly.
  3. Medical Professionals: This lawsuit doesn't just affect the patients; medical professionals who have recommended or inserted the Paragard IUD may also feel the repercussions. They might face questions and concerns from current patients, reconsider their device recommendations, and even potentially become involved in the legal processes if they treated patients who experienced complications.
  4. General Public Perception: Beyond the direct victims, the broader public's trust in medical devices and the processes that approve and monitor them can be impacted by large-scale lawsuits like the Paragard case. Such controversies often ignite discussions about the balance between innovation, regulation, and patient safety.

In essence, while the direct number of individuals experiencing complications from Paragard might be in the thousands, the ripple effects of the lawsuit touch many more lives. Medical professionals, legal practitioners, researchers, and anyone with a vested interest in public health should keep a close eye on the developments of the Paragard IUD lawsuit.

Do I Qualify for the Paragard IUD Birth Control Lawsuit?

For those who believe they may have been adversely affected by the Paragard IUD, understanding the criteria for joining the lawsuit is vital. While each case is unique, there are general factors and conditions that can determine eligibility:

Nature and Severity of Injury

One of the primary criteria is having suffered a significant injury or complication directly linked to the Paragard IUD. This could range from the device fracturing upon removal, leading to surgeries to remove fragments, to other associated complications like infections, organ damage, or inflammation.

Timeline of Events

The timing of the device's implantation, the occurrence of complications, and its removal can all play a role. It's essential to establish that the injuries occurred within a reasonable time frame after the device was inserted or removed.

Direct Link to Paragard

It's crucial to ascertain that the complications or injuries were a direct result of the Paragard IUD and not due to other unrelated medical conditions or factors.

Medical Documentation

Having thorough medical records that detail the injuries, treatments received, surgeries, and any other related medical interventions can significantly strengthen a claim. This documentation can provide concrete evidence of the extent and cause of the injuries.

Awareness and Reporting

If the adverse effects were reported to a healthcare professional and actions were taken (like surgeries or treatments), it further validates the claim.

For many, navigating the complexities of determining eligibility can be daunting. However, at ConsumerShield, we specialize in guiding victims through the initial stages of the legal process. Our team of experts offers free claim reviews, helping individuals understand if their experiences with Paragard qualify them for the lawsuit. We simplify the process, ensuring that victims have the best possible chance to seek the justice and compensation they deserve.

If you believe you or a loved one might have a valid claim, don't hesitate to reach out. We're here to provide the clarity and support you need during this challenging time.

IUD Lawsuit Settlement Amounts: What to Expect

Navigating the legal landscape of medical device lawsuits can be daunting, especially when trying to estimate potential compensation. While every case is unique, several factors influence settlement amounts, and there are preliminary estimates based on previous class actions related to similar medical device lawsuits.

Preliminary settlement estimates for Paragard Lawsuits are as follows:

  • For the most severely affected: Victims who experienced the most severe complications, resulting in significant medical interventions, prolonged treatments, or permanent injuries, could potentially receive settlements ranging from $100,000 to $200,000.
  • If you have moderate complications: Individuals who faced moderate complications, which might have required medical attention but not long-term interventions, can expect settlements in the ballpark of $25,000 to $75,000.
  • If you have lesser injuries: Those who had minimal complications, requiring less intensive medical care and having less lasting impact, might see settlements under $25,000.

Other influencing factors include:

  • Medical Expenses: Tangible costs like surgeries, hospital stays, and medications can be a significant component of the settlement.
  • Lost Wages and Earning Capacity: If the complications led to missed work or impacted future earnings, these losses could be factored in.
  • Pain and Suffering: Non-economic damages such as emotional distress and decreased quality of life play a role in determining compensation.
  • Legal Precedents: Outcomes of early verdicts or settlements can set benchmarks for subsequent cases.
  • Willingness to Settle: The manufacturers' strategy in terms of out-of-court settlements versus court battles can vary based on multiple factors.
  • Strength of Legal Representation: Having an experienced legal team can play a pivotal role in negotiations and the eventual settlement amount.

For those affected by Paragard complications, it's essential to consult with legal professionals who can provide insights specific to your situation. ConsumerShield is dedicated to guiding victims through this intricate process, ensuring they're equipped with the information and resources needed to pursue rightful compensation.


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How Can ConsumerShield Help?

At ConsumerShield, we stand with the victims of Paragard IUD complications. We offer free claim reviews to determine your eligibility for compensation.

Our dedicated team connects you with experienced legal professionals who can guide you through the complexities of the Paragard IUD lawsuit.

Here's a straightforward guide to kick-start your journey with ConsumerShield for the Paragard lawsuit:

Step 1: Fill Out the Online Form

Begin by filling out the free case review form here. Once you have submitted your information, a member of our intake team or a representative from our partnered law firm will promptly contact you to guide you through the subsequent steps.

Step 2: Complimentary Case Assessment

After our initial touchpoint, our experts will undertake a comprehensive case assessment at no charge. During this phase, we'll dive deeper into your circumstances to gauge the viability and potential value of your claim. We're here to address any queries you might have and will walk you through the procedure so you're well-informed about upcoming stages. This assessment is instrumental in determining your eligibility to proceed with a Paragard lawsuit.

Step 3: Pursue the Justice You Deserve

Upon gathering all pertinent details and confirming your eligibility for the lawsuit, you'll be backed by our vast network of seasoned attorneys and medical specialists. These experts, having secured substantial compensations for individuals in similar predicaments, will channel their expertise to champion your cause. They'll manage the legal intricacies, enabling you to center your attention on recovery and personal well-being.

Don't suffer in silence; let us help you find the justice you deserve.

Frequently Asked Questions

  • As of the information provided, there hasn't been a mention of an official recall for the Paragard IUD. However, there are ongoing lawsuits alleging complications and injuries associated with the device.

  • The Paragard IUD is a non-hormonal intrauterine device made with copper. While the device's primary mechanism is to prevent pregnancy using copper's spermicidal properties, there's no information provided in our discussion that directly links the Paragard IUD to copper toxicity in users.

  • Our discussion primarily focused on lawsuits related to injuries and complications from the device, such as fracturing upon removal. While the Paragard IUD is designed to prevent pregnancy, the specifics of suing for an unplanned pregnancy were not covered in our conversation. If you believe you have a valid claim, consulting with a legal expert or a service like ConsumerShield is recommended.

  • While it's technically possible to file a lawsuit without an attorney, it's strongly advised to seek legal representation, especially in complex cases like medical device lawsuits. An experienced attorney or a service like ConsumerShield can provide guidance, ensure that all procedural requirements are met, and significantly improve the chances of a favorable outcome.

  • The timeline for resolving a Paragard lawsuit can vary based on numerous factors, including the specifics of the case, the number of plaintiffs involved, and the legal strategies employed by both sides. As of our last update, bellwether trials are expected to begin in early 2024, which can provide more clarity on potential outcomes and settlement timelines.

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