Current Cases

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.

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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.

LEARN MORE ABOUT HERNIA MESH LAWSUITS

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.

LEARN MORE ABOUT THE ETHICON PHYSIOMESH LAWSUIT

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.

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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.

LEARN MORE ABOUT HE PERFIX PLUG LAWSUIT

The 3DMax hernia mesh lawsuit is against Bard and its subsidiary Davol Inc. The 3DMax is a hernia mesh made from polypropylene. Bard has already faced thousands of lawsuits over its transvaginal mesh and bladder sling products, which are also made from polypropylene. Despite the known risk associated with polypropylene, Bard continues to manufacture the 3DMax with polypropylene.

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The Composix Kugel is a hernia mesh patch created by Bard Davol. The Composix Kugel utilizes a polypropylene base and a permanent PTFE barrier that is stitched to the polypropylene. The Composix Kugel also incorporates and flexible, non-resorbable ring the in middle of the mesh. The polypropylene and the PTFE of the Composix Kugel contract at different rates, causing the mesh patch to deform over time. Additionally, the polypropylene and PFTE can shrink to a size smaller than the center ring, resulting in the ring breaking. Severe injuries, such as bowel perforations are common when the ring breaks within the Composix Kugel.

Learn More About The Composix Kugel Lawsuit

The Ventralex hernia mesh lawsuit is against Bard and its subsidiary Davol Inc. The Ventralex is a hernia mesh patch made from polypropylene. Bard has already faced thousands of lawsuits over its transvaginal mesh and bladder sling products, which are also made from polypropylene. Despite the known risk associated with polypropylene, Bard continues to manufacture the Ventralex with polypropylene.

LEARN MORE ABOUT THE VENTRALEX ST LAWSUIT

C.R. Bard and its subsidiary Davol currently market the Sepramesh. Injuries associated with the Sepramesh include adhesions, pain, bowel adhesions, and infection.

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.

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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.

LEARN MORE ABOUT THE PARIETEX COMPOSITE LAWSUIT