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Teva Defense Verdict — What It Means for Paragard Cases

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Written By
People's Justice Legal Research Team

The Rickard v. Teva Trial — What Happened

On February 5, 2026, the jury in Rickard v. Teva Pharmaceuticals USA, Inc. — the first bellwether trial in MDL 2974 — returned a verdict for Teva on all counts. Plaintiff Pauline Rickard had alleged that her Paragard IUD broke during removal in 2018, causing injury that required surgical intervention, and that Teva failed to warn patients and providers of the device's propensity for arm fracture. After a multi-week trial in Atlanta before Judge Leigh Martin May, the jury rejected plaintiff's failure-to-warn and defective design theories. Teva's key arguments were: (1) Paragard's prescribing information disclosed the risk of arm breakage during removal; (2) the plaintiff's provider's removal technique, rather than the device design, was a contributing cause; and (3) the plaintiff failed to establish that a stronger warning would have changed her or her provider's decision to use Paragard.

What the Defense Verdict Means — and What It Doesn't

The Rickard defense verdict means that the specific jury who evaluated Pauline Rickard's specific case found for Teva. It does not mean that all Paragard cases will lose. Each case in an MDL is evaluated on its own facts, and plaintiffs with stronger fact patterns — particularly clear imaging documentation of fragment retention, multiple major surgeries, and infertility — are meaningfully distinguished from the Rickard case. The defense verdict will likely give Teva greater leverage in global settlement negotiations for lower-tier cases, but it increases the importance of aggressive medical record development and expert testimony for cases in the top injury tiers. Women who suffered infertility, hysterectomy, or major organ damage should not be deterred from pursuing their claims.

Comparable MDL Defense Verdicts — History Shows Recovery Is Possible

Large medical device and pharmaceutical MDLs routinely produce defense verdicts in early bellwether trials. The 3M Combat Arms Earplug MDL saw numerous defense verdicts before a $6 billion settlement. Bayer's Essure MDL produced defense wins before meaningful resolution. In each of these cases, a single defense verdict did not end the litigation — it refined the plaintiff's bar's approach, strengthened subsequent case presentations, and ultimately contributed to a settlement framework that compensated injured claimants. The MDL process is designed to use bellwether trials — including defense verdicts — as data points for both sides. The March and May 2026 bellwether trials will provide those additional data points for Paragard.

Should I Still File After the Defense Verdict?

Yes — if your Paragard broke, you required surgery, and you suffered significant injury, you should still consult an attorney and file a claim if your statute of limitations has not expired. The Rickard defense verdict does not bar your claim or eliminate your right to compensation. MDL 2974 is ongoing. Two more bellwether trials are forthcoming. Settlement negotiations between the parties continue. The critical action item is not waiting: the 2025 breakage-date ruling means statutes of limitations are actively running from your Paragard removal date. Waiting to see how subsequent bellwether trials unfold risks your statute of limitations expiring while the MDL continues. File now, preserve your rights, and let the litigation process play out while your claim is protected.

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Paragard IUD Lawsuit Update 2026

2026 is a pivotal year for Paragard MDL 2974 — the first bellwether trial ended in a Teva defense verdict on February 5, two more trials follow in March and May, and global settlement negotiations are active as both sides assess litigation risk

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Paragard IUD Broken During Removal Lawsuit

Device arm fracture during removal is the central defect in Paragard litigation — when the T-frame's arms snap off inside the uterus, what was a routine office procedure becomes a surgical emergency requiring hysteroscopy, laparoscopy, or in severe cases, hysterectomy

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Paragard IUD Copper Toxicity Lawsuit

Retained copper fragments from a broken Paragard IUD can cause chronic copper exposure, inflammation, and systemic copper toxicity symptoms — an underreported injury type distinct from the mechanical fracture injuries at the center of most MDL 2974 claims

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Paragard IUD Infertility Lawsuit

Infertility caused by a broken Paragard IUD commands the highest tier of damages in MDL 2974 — projected settlements of $100,000 to $380,000 for women who lost the ability to conceive as a direct result of device fracture, surgical complications, or hysterectomy

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Paragard IUD Organ Perforation Lawsuit

Paragard fragments that migrate beyond the uterine cavity can perforate the bowel, bladder, fallopian tubes, and other abdominal organs — requiring major surgery and carrying permanent health consequences that significantly elevate damages in litigation

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Paragard IUD Removal Complications

Paragard removal complications — from arm fracture to organ migration to emergency surgery — represent a spectrum of outcomes from a device marketed as easily and safely removable, and each level of complication may support a product liability claim against Teva

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Paragard IUD Lawsuit Settlement Amounts 2026

Paragard IUD settlement amounts range from $10,000 to $380,000 depending on injury severity — with the Teva defense verdict in February 2026 creating uncertainty while two more bellwether trials in 2026 will further define the litigation's value

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Paragard IUD Statute of Limitations by State

A 2025 MDL ruling established that Paragard statutes of limitations run from the date of device breakage — not symptom onset — making immediate action critical for women whose Paragard broke in 2022, 2023, or 2024

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Who Qualifies for a Paragard IUD Lawsuit?

You may qualify for a Paragard IUD lawsuit if your device broke during removal and you suffered a documented injury — surgery, organ damage, or infertility — with medical records to support the claim and your state's statute of limitations still open

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Parent Case

Paragard IUD Lawsuit Lawsuit

Paragard (T380A copper IUD) was FDA-approved in 1984 and has been used by millions of American women as a hormone-free long-term contraceptive. Women and their doctors began reporting a troubling pattern: when Paragard is removed — a routine office procedure — the device's copper-and-plastic arms snap off inside the patient. The retained fragments can migrate, perforate organs, cause chronic pelvic pain, and require invasive surgery including hysteroscopy, laparoscopy, and in some cases hysterectomy to remove. Women who suffered uterine perforation, organ damage, or infertility from a broken Paragard may have a product liability claim against Teva Pharmaceuticals. The MDL is pending before Judge Leigh Martin May in the Northern District of Georgia. The first bellwether trial (Rickard v. Teva) ended in a defense verdict on February 5, 2026. Two additional bellwether trials are scheduled in March and May 2026. Settlement negotiations are active. Claimants who can document breakage, surgery, and significant injury — especially infertility — have the strongest cases.

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