510(k) clearance history:
Composix Kugel 2001 (510k summary missing from FDA website)
Ventrio 2008 (fully resorbable ring)
Ventralex 2013 (changing to a resorbable ring)
Truvada and other antiretroviral drugs containing the active ingredient tenofovir disoproxil fumarate, TDF, may increase the risk of bone density loss, bone fractures, renal impairment, and kidney failure. Our Truvada lawyers are currently investigating claims where individuals suffered these side effects from using Truvada.
Deadly cardiovascular problems from the use of Uloric, a drug commonly prescribed for the treatment of gout. Our Uloric lawyers are currently investigating claims for individuals who experienced a heart attack, heart failure, stroke, or other cardiovascular complications from the use of Uloric.
Defective combat earplugs provided to the US Military were designed too short and did not fit properly to protect the inner ear from damage. Our 3M lawyers are currently investigating claims for US veterans that utilized 3M’s Combat Arms Earplugs and have subsequently experienced hearing loss or tinnitus.
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.
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 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.
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.
510(k) clearance history:
Composix Kugel 2001 (510k summary missing from FDA website)
Ventrio 2008 (fully resorbable ring)
Ventralex 2013 (changing to a resorbable ring)
8101 College Blvd Suite 260
Overland Park, KS 66210
Local: 913.385.5400
Toll Free: 1.800.701.3672