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Litigation Stage Tracker
Active Filing

Paragard IUD

BorderlineFILING
MDL 2750Device
3,600+
Total Cases

Causation

Plaintiffs allege the Paragard IUD's polyethylene frame becomes brittle after prolonged implantation, causing the device arms to fracture during standard removal procedures. The T-shaped design creates stress points at the arm-body junction that weaken over time. Fractured pieces embed in the myometrium, requiring hysteroscopy, laparoscopy, or hysterectomy for removal. FDA MAUDE database documents hundreds of breakage reports. Plaintiffs argue defendants knew of the breakage risk from post-market surveillance data but failed to update warnings, modify the design, or instruct physicians on modified removal techniques.

Defendants

EntityRoleNote
Teva PharmaceuticalsFormer ManufacturerManufactured and marketed Paragard before sale to CooperSurgical
CooperSurgical Inc.Current ManufacturerAcquired Paragard from Teva in 2017 for $1.1B — current label holder
The Cooper CompaniesParent CompanyParent of CooperSurgical — assumed Paragard product liabilities

Litigation Timeline

1984
Paragard IUD first approved by FDA
2017
CooperSurgical acquires Paragard from Teva for $1.1B
2020
First wave of breakage lawsuits filed in federal courts
2023
Bellwether discovery pool selected
2025
Mediation initiated — global settlement discussions
2026
3,600+ cases pending. Mediation ongoing

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Key Facts

Status
active

Geographic Exposure

·N.D. Ga. (MDL 2974, Judge May)
·Nationwide filing — all 50 states
·Parallel state court actions in NJ and CA

Eligibility Criteria

  • Had a Paragard copper IUD implanted
  • Device broke during removal attempt
  • Required surgical intervention to remove retained fragments
  • Suffered perforation, infection, ectopic pregnancy, or infertility
  • Experienced heavy bleeding or pain from embedded device fragments