Valsartan nationwide has been contaminated with the impurity NDMA and NDEA. Both of these impurities can cause severe side effects, such as cancer formation or liver failure. As a result, millions received a recall letter from Humana. The FDA has confirmed that the contaminated valsartan originated in China and India. Learn more about the dangers and potential side effects of ingesting contaminated valsartan. Our valsartan lawyers are currently investigating and filing lawsuits related to liver and bowel cancer that developed after valsartan use.
We are now investigating all hernia mesh claims, even if you don't know what hernia mesh was implanted. Learn more about the most dangerous types of hernia mesh. Severe hernia mesh complications are occurring even with hernia meshes that have not been recalled.
The C-Qur hernia mesh was developed by Atrium Medical Corporation to be utilized during hernia repairs. The C-Qur hernia mesh has an Omega 3 fatty acid layer that dissolves in the patients body over several months to years. The Hollis Law Firm represents clients in lawsuits who have experienced severe complications after being implanted with the C-Qur hernia mesh. Lawsuits regarding the C-Qur hernia mesh include infections, organ perforation, rejection, additional surgeries, pain and systemic skin rashes.
Ethicon's Physiomesh was developed for hernia repair. Physiomesh was recalled from the global market in 2016, because of high rates of complications. Complications of Physiomesh include hernia recurrence and additional surgeries. The Hollis Law Firm represents those who have experienced complications with Physiomesh.
The Proceed hernia mesh is a light-weight polypropylene mesh with a resorbable Oxidized Regenerated Cellulose (ORC) fabric attached to the polypropylene. The cellulose is bonded to the polypropylene with polydioxanone (PDS). Johnson & Johnson and Ethicon previously recalled lots of the Proceed mesh, because of the cellulose layer delaminated from the underlying polypropylene. The Proceed's ORC layer is ineffective and frequently results in severe bowel injuries.
The Bard PerFix Plug is utilized to repair inguinal hernias. Many have experienced debilitating pain after being implanted with Bard's PerFix Plug. Removal of Bard's PerFix Plug can be very difficult, and many men have lost a testicle in the process.
Covidien later decided to attach a thin collagen layer to the Parietex, creating the Parietex Composite (PCO). The thin collagen coating of the Parietex Composite was intended to increases the meshes handling, while also protecting the patient's bowels from the harmful effects of the polyester. Unfortunately, the collagen barrier of Covidien's Parietex Composite does nearly nothing to protect a patient's underlying organs. Life-threatening bowel complications are associated with the Parietex Composite hernia mesh.
The Hollis Law Firm handles cases for people who have been injured by harmful prescription drugs and medical devices. Clients are represented on a contingent fee basis, which means that the client is not responsible for paying costs or fees unless there is a recovery. All aspects of the attorney-client relationship are kept strictly confidential. We take pride in the fact that we respond to client inquiries and phone calls personally and promptly.Learn More About The Firm