Atrium C-Qur Mesh

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Atrium C-QUR Mesh Lawsuits

Atrium, owned by Maquet Cardiovascular has recalled the Atrium C-Qur Mesh hernia patch back in 2013. Even though there was a recall, none of Atrium’s hernia mesh products were actually pulled from the market. Atrium simply wrote a letter notifying doctors to be aware that the mesh’s coating could stick to the packaging and peel off the mesh itself. The purpose of the the coating is to prevent the polypropylene portion of the mesh from coming into direct contact with a patient’s organs. Unfortunately, physicians have reported to the FDA experiences of the coating peeling off upon implantation or within days after implantation

C-QUR-V-Patch

Atrium C-Qur Hernia Mesh Problems

Atrium first introduced C-Qur Mesh (pronounced Atrium “Secure”) in 2005, through the controversial 510(k) FDA approval system, which allowed the medical device to be introduced without rigorous pre-market research and studies.

Despite signs of potential problems with the Atrium C-Qur mesh design, the manufacturer has introduced a variety of similar products for use in hernia repair, chest wall reconstruction and treatment of traumatic or surgical wounds, including:

  • Atrium C-Qur Mesh
  • Atrium C-Qur Mosaic
  • Atrium C-Qur TacShield
  • Atrium C-Qur V-Patch
  • Atrium C-Qur Centrifx
  • Atrium C-Qur FX Mesh (formerly C-Qur Lite)

All of these products are constructed out of an Atrium polypropylene mesh, with an outer coating of gel made from omega 3 fatty acids, called the O3FA layer.

Risks and Symptoms

Those who have been implanted with Arium’s C-Qur mesh may suffer from various complications, including:

  • Infections
  • Allergic Reactions
  • Abdominal Pain, Bowel Adhesions, Ulcers or Organ Perforation
  • Mesh Erosion or Failure
  • Revision Surgery

Several studies have investigated the complications associated with Atrium’s C-Qur hernia mesh. A study conducted in Belgium had to be stopped early because of an unacceptably high rate of C-Qur hernia mesh infections. A separate study also experienced infections in nearly every C-Qur hernia mesh that was implanted. 

Recently, the FDA sued Atrium and Maquet for introducing adulterated medical devices into interstate commerce. The FDA was granted a permanent injunction against the facility that manufacturers the C-Qur hernia mesh. Atrium’s hernia mesh was not pulled off the market though. Many providers have discontinued using the C-Qur hernia mesh; however, it is still being implanted at some hospitals.

If you, a friend or family member has suffered infections, gastric ulcers or other hernia mesh complications, request a free consultation and claim evaluation. Each case does have a statute of limitations, or deadline by which any Atrium C-Qur lawsuit must be filed, so it is important to review any potential claims as early as possible to make sure that your legal rights are protected. Contact The Olinde Firm now, for your free case evaluation

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If you believe that you or someone you know may have had Atrium C-Qur Mesh implanted®, please contact us now for a free, confidential consultation.

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Phone: (504) 587-1440
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