LAWSUITS NEWS & LEGAL INFORMATION
Atrium C-QUR Hernia Mesh Causing Pain and Infection
Santa Clara, CA: Allegations that the Atrium C-Qur hernia mesh causes severe health effects including pain and injury in people who’ve undergone the surgery, are being made. Additionally, plaintiffs who have filed lawsuits claim that Atrium was aware of the problems with the mesh but did nothing to warn the medical community.
Specifically, Atrium Medical is being accused of producing a defective product by plaintiffs who state that their C-Qur hernia mesh caused them severe pain, internal injuries, an antibiotic-resistant infection and septic shock, after the patch “folded up.”
As a result, plaintiffs are allegating the C-Qur hernia mesh is not safe to use for its intended purpose.
Approved by the FDA in March 2006, for use in hernia repair, chest wall reconstruction and to repair traumatic or surgical wounds, Atrium C-Qur has subsequently been linked to a host of medical adverse events and side effects.
As a consequence, the FDA issued a warning letter to Atrium in October 2012, citing the company for failing to investigate and respond to complaints about C-QUR mesh infections and failure.
A recently filed complaint describes the associated adverse health effects in the following manner : “The injuries, conditions and complications suffered due to Defendants’ C-Qur Meshes include, but are not limited to, foreign body reaction, rashes, infection, adhesions, organ perforation, inflammation, fistula, mesh erosion, scar tissue, blood loss, dyspareunia, neuropathic and other acute and chronic nerve damage and pain, abdominal pain, nausea, vomiting, [and] kidney failure. ”
It continues, “[I]n many cases the patients have been forced to undergo intensive medical treatment, including but not limited to operations to locate and remove the C-Qur Mesh, operations to attempt to repair abdominal organs, tissue and nerve damage, the use of narcotics for pain control and other medications, and repeat operations to remove various tissues that are contaminated with the C-Qur Mesh.”
The number of people thought to have suffered adverse events as a result of having the C-QUR Mesh implant is in the thousands.
Last updated on
Specifically, Atrium Medical is being accused of producing a defective product by plaintiffs who state that their C-Qur hernia mesh caused them severe pain, internal injuries, an antibiotic-resistant infection and septic shock, after the patch “folded up.”
As a result, plaintiffs are allegating the C-Qur hernia mesh is not safe to use for its intended purpose.
Approved by the FDA in March 2006, for use in hernia repair, chest wall reconstruction and to repair traumatic or surgical wounds, Atrium C-Qur has subsequently been linked to a host of medical adverse events and side effects.
As a consequence, the FDA issued a warning letter to Atrium in October 2012, citing the company for failing to investigate and respond to complaints about C-QUR mesh infections and failure.
A recently filed complaint describes the associated adverse health effects in the following manner : “The injuries, conditions and complications suffered due to Defendants’ C-Qur Meshes include, but are not limited to, foreign body reaction, rashes, infection, adhesions, organ perforation, inflammation, fistula, mesh erosion, scar tissue, blood loss, dyspareunia, neuropathic and other acute and chronic nerve damage and pain, abdominal pain, nausea, vomiting, [and] kidney failure. ”
It continues, “[I]n many cases the patients have been forced to undergo intensive medical treatment, including but not limited to operations to locate and remove the C-Qur Mesh, operations to attempt to repair abdominal organs, tissue and nerve damage, the use of narcotics for pain control and other medications, and repeat operations to remove various tissues that are contaminated with the C-Qur Mesh.”
The number of people thought to have suffered adverse events as a result of having the C-QUR Mesh implant is in the thousands.
Atrium C-Qur Hernia Mesh Legal Help
If you or a loved one has suffered similar damages or injuries, please click the link below and your complaint will be sent to a lawyer who may evaluate your claim at no cost or obligation.Last updated on
ATRIUM C-QUR HERNIA MESH LEGAL ARTICLES AND INTERVIEWS
Plaintiff Claims C-Qur Mesh Biologically Incompatible with Human Tissue
Something Fishy Allegedly Going on with Atrium C-QUR Mesh
Surgical Mesh Lawsuit to Proceed
February 19, 2017
Concord, NH: He may have the same name as the long-dead soul singer, but James Brown does not feel good about the C-Qur abdominal mesh used for a hernia repair and the plaintiff, through his surgical mesh lawsuit, has plenty to say about it. READ MORE
Something Fishy Allegedly Going on with Atrium C-QUR Mesh
January 28, 2017
Concord, NH: A lesser-known hernia mesh that is beginning to attain some traction in legal circles is Atrium C-QUR Hernia Mesh, a product approved by the US Food and Drug Administration (FDA) in 2006. Akin to other mesh products made by competing manufacturers for hernia repair, plaintiffs are filing lawsuits alleging complications. READ MORE
Surgical Mesh Lawsuit to Proceed
December 23, 2016
Providence, RI: A Rhode Island man who received recalled abdominal mesh just prior to a product recall in 2005, will see his surgical mesh lawsuit go forward after a Rhode Island judge refused to dismiss the case. READ MORE
READ MORE Surgical Mesh Settlements and Legal News
READ MORE Defective Products Settlements and Legal News
READ MORE Drugs/Medical Settlements and Legal News
READ MORE Personal Injury Settlements and Legal News
READ MORE Defective Products Settlements and Legal News
READ MORE Drugs/Medical Settlements and Legal News
READ MORE Personal Injury Settlements and Legal News