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Paragard IUD Device Failure
Medical Devices

Paragard IUD Device Failure

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Case Overview

The Paragard IUD is a copper intrauterine device used for long-term birth control. While marketed as safe and hormone-free, numerous women have reported the device breaking during removal, leaving fragments embedded in the uterus. These broken pieces can migrate through the uterine wall, causing perforation, infection, and the need for invasive surgical procedures to remove the fragments.

Health Risks & Injuries

  • Device breakage during removal
  • Uterine perforation
  • Ectopic pregnancy
  • Infection and sepsis
  • Embedment in uterine wall
  • Pelvic inflammatory disease
  • Infertility
  • Need for surgical intervention including hysterectomy

Who Qualifies

  • Women whose Paragard IUD broke during removal
  • Those who experienced device migration or perforation
  • Women who required surgery to remove IUD fragments
  • Those who suffered complications from a fractured Paragard device

Current Litigation Status

The Paragard IUD lawsuits are centralized in MDL No. 2974 in the Northern District of Georgia. Thousands of lawsuits have been filed against Teva Pharmaceuticals and CooperSurgical, alleging that Paragard's design makes it prone to fracture during routine removal. Bellwether cases selected for trial are being prepared. New claims continue to be filed as more women learn that their complications may be linked to a fractured Paragard device.

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