Official and authoritative background links used for intake education.
Paragard IUD lawsuit documentation and intake checklist
Paragard reviews focus on IUD implant and removal records, documentation of device fracture or breakage, and injury or surgical records related to the removal complication.
According to the claims, the device fractures when it is removed, resulting in catastrophic injuries and the need for surgery. Claimants contend that Paragard is defective and that the manufacturers failed to appropriately warn about the potential of device breakage and damage.

Pain, infertility, injuries from broken IUD pieces imbedding in organs, need for surgery
Teva Pharmaceuticals USA Inc., Teva Women’s Health Inc., Teva Women’s Health LLC, Teva Branded Pharmaceutical Products R&D Inc., The Cooper Companies Inc. and CooperSurgical Inc.
MDL 2974 in the Northern District of Georgia
- Perforation of the uterus or cervix
- Inflammations and allergic reactions to IUD pieces left in the body
- IUD migration
- IUD pieces missing or lodged in organs
- Infertility
- Need for surgery such as hysterectomy, laparoscopy or laparotomy
- Pain
- Infection
- Broken IUD pieces cannot be removed
Suits allege that the device broke when it was removed, resulting in injuries.
“Paragard removal is noninvasive and can be done by a healthcare professional during a typical office visit in just a few minutes,” according to Cooper Surgical’s website.
According to the instructions for removal given in the prescribing material, the device’s arms are designed to fold up when removed.
However, according to complaints filed by women, Paragard shattered during removal, leaving shards of the IUD in their bodies. The device had to be removed and issues treated in some women, which necessitated surgery.
Free Case Review
In December 2020, the Judicial Panel on Multidistrict Litigation in the Northern District of Georgia presided over by Judge Leigh Martin May, merged dozens of claims from across the country. Trials have yet to be scheduled as of January 28, 2021.
Case Review Form
Campaign guidance, records, and sources
Review the supporting information below before or after completing the private campaign form.
A practical checklist to help organize useful details before review.
Reviewed for intake accuracy by AMMS Compliance Team
Records and details that may help
- Insertion and removal records identifying the Paragard device (batch or lot number if available)
- Operative records documenting device breakage, arm fracture, or embedded components during removal
- Post-removal surgical records, pathology reports, and treating physician information
- Any complications experienced before removal, such as pain, migration, or partial expulsion
Sources used for intake education
These official references are provided for background education only. They do not replace medical or legal advice.
- FDA Paragard IUD device informationFDA information on IUD devices including safety reporting and device manufacturer contacts.
1. Submit the intake form
Share your contact details and answer the existing campaign-specific questions.
2. Organize supporting details
Gather the records, dates, communications, and other details listed for this campaign.
3. Intake follow-up
AMMS or an authorized intake partner may contact you for missing or clarifying details.
4. Legal review if appropriate
Qualified legal professionals decide whether a claim can move forward. AMMS does not provide legal advice or guarantee results.
Frequently asked questions
What does Paragard arm fracture mean for an injury review?
Paragard IUDs have plastic arms that can break during removal, leaving fragments that may require additional surgery. Operative records documenting such breakage are important for intake review.
Can I submit a review if I had the Paragard removed years ago?
Yes. The timing of the removal and complication is important context, but you can still submit intake information regardless of when the removal occurred.


