Mass Tort Lawyers

Women who used popular Hair Straightening Products may have been placed at a higher risk for Uterine Cancer. Did you or a loved one develop uterine cancer after using L’Oreal or other hair straighteners? Shamis Gentile is currently investigating these matters. If you think you have a case, get in touch today for a free consultation. You may be eligible for compensation.

As we speak, the attorneys at Shamis & Gentile, P.A. are investigating cases from veterans from around the country who suffered partial or total hearing loss as a result of being given defective 3M Combat Arms Earplugs. These earplugs were distributed by the U.S. military for many thousands of soldiers, including those headed to combat zones, from 2003 to 2015. The problem with these particular earplugs was a design flaw, which rendered them too short to be properly inserted into the ear canal. This, in turn, made it impossible for the earplugs to provide the proper amount of protection and, ultimately, led to significant hearing damage and hearing loss for the unfortunate veterans who wore them.

Anyone that was injured after exposure to toxic water at camp lejeune between 1953 & 1987 may be eligible for compensation. If you attended Camp Lejeune between 1953 & 1987 and have experienced or developed health problems, contact Shamis & Gentile, P.A. today for a Free case review.

If you were affected by Roundup weed killer or if you lost an immediate family member, we can help you to get compensation for the financial burden it caused for you and your family.

If you used Paraquat herbicide and have experienced or developed health problems, contact Shamis & Gentile, P.A. today for a Free case review

Shamis & Gentile, P.A. are your skilled mass tort attorneys for your hernia mesh lawsuit as they have been representing clients in these cases for many years. A hernia mesh lawsuit is yet another example of complications arising from design defects. It has been frequently seen, within a few years of receiving a hernia mesh implant, many patients begin experiencing a variety of adverse symptoms, including complications with the implanted surgical mesh.

If your child of 18 or younger has suffered from Suicide, attempted suicide, or developed an eating disorder, body dysmorphia, or other mental health condition due to social media usage, contact Shamis & Gentile, P.A. for a Free case review.

Contact Shamis & Gentile, P.A. to find out if you or a loved one may be eligible for a Philips CPAP lawsuit payout after exposure to toxic particles and gasses released by the defective sound abatement foam

If you or a loved one used Talcum Powder and have developed ovarian cancer and other gynecological cancers, contact Shamis & Gentile, P.A. today for a Free case review.

The lawyers of Shamis & Gentile, P.A. have the ability and know how to successfully litigate transvaginal mesh lawsuits. There are many occasions from which it is necessary to bring a transvaginal mesh lawsuit, due mostly in part to the alarming reports of serious complications from these treatments. It has become such an issue that the FDA issued a public safety notice in late 2008 about vaginal mesh devices and in 2011 warned that complications from TVM products are not rare, and that alternative treatments may be preferable. In 2012, the FDA issued a requirement that manufacturers of the products conduct new clinical trials to assess the risk of serious complications. This has led to a huge transvaginal mesh recall.

There are many brands that are being reviewed for potential recovery against, among the most common being Bard G2 IVCfilter, Bard Recovery IVC filter (manufactures of the Eclipse brand IVC filter) and Cook IVC filter (manufacturers of the Celect brand IVC filter and Gunther Tulip filter). These companies failed to adequately warn about the risks of the problems and negligently designed a defective and unreasonably dangerous IVC filter. It is our opinion that the manufactures will ultimately be forced to pay substantial financial compensation to resolve these cases.

In February 2022, Florida-based medical device company Exactech issued a recall on over 150,000 knee, ankle and hip replacement devices. If you or a loved one has received a knee replacement, hip replacement, or ankle replacement since 2004, one of these non-conforming devices may have been used in your procedure. If this is the case, you may be at risk of premature wear on the devices or bone loss. You may even need revision surgery. If you are among the thousands of Americans in this position, you should reach out to an Exactech recall lawyer, as you may be eligible to join an ongoing Exactech lawsuit.