1. Submit the intake form
Share contact details, diagnosis information, exposure history, and the campaign you want reviewed.
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
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.
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.
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.
These official references are provided for background education only. They do not replace medical or legal advice.
Share contact details, diagnosis information, exposure history, and the campaign you want reviewed.
Gather medical records, product history, proof of exposure, and timeline information that may help reviewers understand the claim.
AMMS or an intake partner may contact you for clarifying details before any potential legal review.
Qualified legal professionals decide whether a claim can move forward. AMMS does not provide legal advice or guarantee results.
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.
Yes. The timing of the removal and complication is important context, but you can still submit intake information regardless of when the removal occurred.