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Victims who have suffered from injuries or adverse side effects due to the Paragard® intrauterine birth control device (IUD) are urged to get a free, private case evaluation

Victims who have suffered from injuries or adverse side effects due to the Paragard® intrauterine birth control device (IUD) are urged to get a free, private case evaluation

Paragard® birth control linked to serious side effects, including:

  • device breakage
  • removal by hysteroscopy
  • removal by hysterectomy
  • inability to remove the device
  • surgical removal

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Thousands of women are experiencing health-related complications or have been injured by the Paragard® IUD

When implanted, the device can perforate or damage the uterus, leading to infection or scarring.

Additionally, when being removed, the paragard device has been found to fracture or break, leading to serious injuries or even more extensive surgeries to remove the device. Since the 1980s, thousands of women have used the Paragard® IUD.

The device can be implanted non-surgically at a doctor's office and is effective for up to 10 years, or until a patient has the device removed.

However, a peer-reviewed medical journal soon began to find evidence of thousands of women suffering from serious injuries during the removal of the device.

The Paragard® IUD website claims that their device can be difficult to remove "because it is stuck in the uterus" and that "surgery may sometimes be needed to remove paragard". During removal, however, parts of the Paragard® IUD device may break, which could lead to more surgeries. 

Additionally, the Paragard® IUD device may break on its own prior to removal, which can cause patients to experience severe pain.

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The Hidden Dangers Behind Paragard®

Since the 1980s, thousands of women have used the Paragard® birth control IUD. The device can be implanted non-surgically at a doctor's office and is effective for up to 10 years, or until a patient has the device removed. However, a peer-reviewed medical journal soon began to find evidence of thousands of women suffering from serious injuries during the removal of the device.

The Paragard® websites claims that their device can be difficult to remove "because it is stuck in the uterus" and that "surgery may sometimes be needed to remove Paragard®". During removal, however, parts of the device may break, which could lead to more surgeries. Additionally, the device may break on its own prior to removal, which can cause patients to experience severe pain.

CLASS ACTION LAWSUITS AGAINST PARAGARD® BEGIN
FEBRUARY 2020

PARAGARD® COMPLICATIONS APPEAR IN MEDICAL JOURNALS
OCTOBER 2015

PARAGARD® DEVICE FIRST RELEASED FOR SALE
APRIL 1988

PARAGARD® DEVICE BECOMES FDA APPROVED
NOVEMBER 1984

Please seek the advice of a medical professional before making health care decisions. This website is not associated with Paragard® or any government agency.