C-QUR MESH ALERT

YOU MAY BE ENTITLED TO COMPENSATION AND DAMAGES FOR YOUR INJURIES – WE ARE AVAILABLE TO ASSIST YOU IN YOUR RECOVERY

Class Action Lawsuits Filed Nationwide on Behalf of Victims Injured by C-QUR Mesh

According to multiple class action lawsuits filed across the country, C-QUR Mesh failures have caused serious side effects including infections, internal injuries and mesh adhesion

If you or a family member has or had a C-QUR Mesh implanted and have been injured, you may be entitled to compensation.

DON’T DELAY – CALL US 888-252-0048 OR COMPLETE AND RETURN THE CLAIM FORM
C-QUR MESH ALERT

C-QUR MESH ALERT

  • Our firm is vigorously pursuing this matter.
  • Our clients have received millions of dollars in medical device lawsuits.
  • No Charge or Obligation for Our Experienced Attorney Review

CONTACT US NOW! Do Not Delay As The Applicable Statute Of Limitations May Result In A Complete Bar To Your Claim Regardless Of Its Merit.

About C-QUR Mesh

C-QUR Mesh is manufactured by Atrium Medical Corporation and was approved by the FDA in 2006 for hernia repair, chest wall reconstruction and the repair of surgical wounds. In July 2013, Atrium voluntarily recalled the hernia repair implants due to the coating of C-QUR Mesh sticking to the inner package lining when exposed to excessive humidity for an extended period of time.

Class action lawsuits have been filed nationwide against Atrium alleging plaintiffs have suffered serious side effects due to the implantation of C-QUR Mesh. Many plaintiffs have experienced infections, internal injuries to nearby organs, nerves and/or blood vessels, mesh adhesion to the intestines, chronic pain and recurring hernia. The numerous lawsuits claim Atrium failed to conduct adequate research and testing of the C-QUR Mesh and misled the public when it marketed the product as safe and effective knowing it could cause serious medical problems.

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