When choosing an intrauterine device (IUD) as your form of birth control, you rely on manufacturers to provide safe, dependable products, and to be forthcoming about the severity of potential risks. However, thousands of women with Paragard® and health professionals have reported severe health problems to the FDA after the women received the device, including at least 15 deaths. Eligibility requirements must be met to file a Paragard lawsuit.
FIDELMA FITZPATRICK APPOINTED LEADERSHIP POSITION FOR NATIONAL PARAGARD LAWSUIT
Feb. 24, 2021
Motley Rice medical attorney Fidelma Fitzpatrick is a member of the Plaintiffs’ Executive Committee of the Paragard MDL, and will help lead the national consolidated litigation for women who suffered severe effects allegedly caused by the IUD. Read more.
Motley Rice birth control defect lawyers are investigating the safety and potential harms caused by the intrauterine contraceptive device Paragard®, manufactured by CooperSurgical.
Contact an attorney about Paragard litigation
If you or a loved one underwent the Paragard birth control procedure and experienced severe complications, you may have a claim. Complete this form or call 1.800.768.4026 for more information and to discuss your potential Paragard lawsuit.
Motley Rice has extensive experience litigating for women who have suffered serious injuries and adverse effects related to birth control, including medical attorney Fidelma Fitzpatrick’s role as lead counsel of the Plaintiffs’ Executive Committee for more than 32,000 Essure® cases coordinated in California state court.
Paragard is a T-shaped, hormone-free, device made of flexible plastic with a thin layer of copper that serves as the device’s active ingredient by preventing sperm from reaching the egg and fertilizing it. The device is placed inside the uterus to prevent pregnancy. It is removable, and can last up to 10 years, according to the manufacturer. However, severe complications can occur, particularly if the device migrates or falls out, or pierces the uterine wall.
Potential Paragard Side Effects
The FDA first approved Paragard in 1984. The FDA approved revisions for Paragard’s prescribing label in 2005, expanding the type of recommended patients from women in monogamous relationships with at least one child, to women in all stages of reproductive life from age 16 to menopausal.
Women with Paragard and their medical providers have made more than 40,000 reports to the FDA in the 30 years since Paragard was approved, according to publicly available data in the FDA Adverse Events Reporting System (FAERS) database, which is intended to help identify safety concerns related to marketed products. Of the tens-of-of thousands of reports, more than 15,500 have involved serious complications and at least 15 deaths. The agency received 7,273 reports in 2019 alone, according to FAERS.
Severe Paragard complications may include:
- IUD breakage upon removal
- Surgeries, including hysterectomy
Our experience with medical device litigation
Our attorneys have experience representing women alleging harm by defective medical devices, including being co-lead counsel for the Mirena® IUD multidistrict litigation, lead counsel for coordinated cases involving permanent birth control device Essure®, and serving on the Plaintiff’s Steering Committee for Nuvaring® multidistrict litigation. Read more on our birth control litigation experience.