Hernia Patch Litigation Court Will Hear Claims by Patients With Non-Recalled Hernia Mesh and Patch Devices Manufactured by Bard, Inc. and Davol, Inc.
The court assigned to oversee the nationwide hernia patch and mesh lawsuits will hear claims of patients with both recalled and non-recalled hernia mesh and patch devices.
Over the last few years a number of patients have brought hernia mesh patch lawsuits against C.R. Bard, Inc., and Davol, Inc. alleging that their hernia mesh patch devices were defective and caused injuries. A large number of the claims were brought after an FDA hernia patch recall including claims based on defects in hernia mesh patches non-recalled hernia mesh patch devices.
Hernia patch lawsuits from across the United States have now been consolidated into a single court for all pretrial proceedings. In a recent ruling the court clarified the scope of the consolidated proceedings to include both recalled and non-recalled devices.
The federal Multi-District Litigation court has announced that it will hear hernia mesh and patch lawsuits involving both recalled and non-recalled devices manufactured by C.R. Bard, Inc., and Davol, Inc., including the following;
-All nine (9) models of Bard ComposiX Kugel Hernia Patches (Product Codes 0010201 through 0010209);
-All other Davol hernia patches with PET rings, including the Bard Kugel Hernia Patch; Bard VentraleX Hernia Patch; Bard CK Parastomal Patch; and Bard Modified Kugel Patch; and
-Other Davol hernia meshes composed of layers of polypropylene and ePTFE, including the Bard Composix E/X Mesh.
Hernia patch lawyers at The Johnson Law Firm, a national law firm representing a large number of patients who have been injured by the recalled Bard Composix Kugel Hernia Mesh Patch are evaluating claims by patients with non-recalled hernia patch and mesh products manufactured by Davol, Inc. and C. R. Bard, Inc. Hernia patch lawsuit information, hernia patch class action information, hernia patch recall information and claims evaluations are available at no cost to affected patients at and toll free at 1-866-374-0338.
Many people today are undergoing different kinds of surgical treatments and hip replacement surgeries. Hip implant is a surgical procedure that assists in completely removing the diseased cartilage and bone of the hip joint. In addition, it also replaces all these by means of artificial implants. The main purpose of undergoing a hip recall surgery is to get absolutely rid of the serious hip joint’s arthritis. Osteoarthritis is the most common kind of arthritis and is most recurrent among the elderly. Besides osteoarthritis, trauma to the hip, kidney problems, congenital abnormalities, rheumatoid arthritis and necrosis of the hip bone are various other common causes that necessitate a hip recall surgery.
Stryker Corporation is one of the leading manufacturers of orthopedic implants. Over the past three years, there have been frequent patient complaints regarding defective hip and joint replacements from Stryker. Patients have complained about pain, difficulty in walking, uneven component wear, bone fractures, component breakage and discomfort.
Recurrent patient complaints resulted in FDA intervention in the matter and the FDA inspected the company’s facilities at New Jersey and Cork, Ireland. The inspections unearthed many problems, such as striking inconsistencies in manufacturing and quality control and instances of bacterial contamination. Despite the grave risk that these glaring inconsistencies can pose to patients’ health, Stryker failed to discover the source of the bacteria. In response to repeated FDA warnings, Stryker announced Hip Implant Recall of two of its parts used in the Trident line.
If you or your loved one has been injured as a result of defective Stryker implant and is experiencing pain at the site of the implant, broken bones, difficulty walking or Staph infection after the surgery, you must immediately seek the professional advice of a hip recall lawyer. A Stryker recall lawyer will help you in filing a hip replacement lawsuit or hip recall lawsuit and provide effective legal representation. You can sue the company for defective implants and also claim compensation for your suffering and various medical expenses.
Transvaginal mesh is a type of fabric used to treat pelvic prolapse, bladder prolapse and other similar problems in women. Often, studies have shown that transvaginal mesh has been more effective in treating these problems than the traditional method of stitching the connective tissue in the vaginal wall muscle back together. However, a disturbing number of incidents have been reported lately in which women that have undergone transvaginal mesh surgery have experienced serious health problems. That has led many to contact transvaginal mesh lawyers.
The FDA first released a public health notification in 2008 that alerted healthcare providers to the possible danger of transvaginal mesh as an increasing number of serious health problems possibly caused by the mesh were being reported. More recently in 2011, the FDA issued a public notice to doctors. This notice informed them that there were nearly 3,000 injuries related to transvaginal mesh between 2008 and 2010.
If you are in the Miami area and believe that you have been the victim of an improper transvaginal mesh surgery, you should consider contacting a Miami Medical Malpractice Lawyer. Medical malpractice happens when a healthcare professional is negligent in performing their duties, such as ignoring public health warnings or making a mistake during surgery.
The FDA has said that there are a number of factors that contribute to complications caused by transvaginal mesh surgery. These complications may include the type of material used in the mesh, the size and shape of the mesh, as well as the procedures used during surgery. If a doctor used an improper material, did not take care to use the right size and shape, or followed improper procedures, that may be grounds for medical malpractice.
Moreover, a doctor may have committed medical malpractice if you were not informed of the dangers of transvaginal mesh. Since 2008, the FDA has made sure that healthcare providers were well-informed of the risks related to the surgery. But even before 2008, there were reports and studies showing that transvaginal mesh surgery may cause substantial complications.
By contacting a Miami medical malpractice attorney and transvaginal mesh lawyers, you may be able to collect compensation for injuries caused by an improper transvaginal mesh procedure. This compensation may include not only compensatory damages but punitive damages as well. Compensatory damages may include medical expenses as well as compensation for pain and suffering. Punitive damages, on the other hand, are meant to punish bad behavior.
Medical malpractice is a complex area of law. There are many rules and regulations governing it, and it often has a language all its own that may seem confusing, if not intimidating, to those not well-versed in it. By working with a Miami medical malpractice attorney and with transvaginal mesh lawyers, it may be possible to successfully navigate the judicial system and secure a fair result. After all, those who suffer from an improperly done transvaginal mesh procedure or a mistake during surgery do not deserve to suffer a financial injury in addition to their physical pain.
Research shows that around 20 million Americans have osteoarthritis, which often occurs in the hip joint. Osteoarthritis is a clinical syndrome in which low-grade inflammation results in pain in the joints, caused by abnormal wearing of the cartilage that covers and acts as a cushion inside joints and destruction of synovial fluid that lubricates those joints. The condition is characterized by pain while walking, standing and bearing weight; stiffness in the joints and decreased mobility. In cases where the cartilage gets thinned due to osteoarthritis, a hip replacement surgery may be unavoidable.
Stryker offers a large range of orthopedic components that are used for surgical implants. However, the company has had problems with its hip devices since January 2005 when it began receiving complaints from patients who had received the implants. The problem was two-fold involving serious defects in the manufacturing as well as the designing process. Frequent problems necessitated FDA intervention in the matter. The FDA inspected the company facilities at New Jersey and Ireland, from where most of the Stryker hip implants to the US are produced.
In its first letter, the FDA cited several violations at the Cork plant, including missed deadlines to fix failures in following procedures for testing problematic products and documenting risk. In its second letter, FDA warned Stryker about its failure to implement adequate corrective and preventive actions in order to prevent recurrence of non-conforming product and other quality problems. In response to the FDA warning, Stryker announced a hip implant recall & knee implant recall of two Trident implant parts: the Trident Actabular PSL Cup and the Trident Hemispherical Cup.
If you or your family member has a Stryker hip implant and have experienced squeaking noises, joint pain or required a replacement of your Stryker implant due to mechanical defects, please contact a Stryker recall lawyer immediately. A Stryker hip recall lawyer will address all your concerns on the subject and guide you through your legal rights.
A qualified and experienced Stryker hip attorney can be contacted at the Barton Law Firm. This firm is recognized as a preeminent law firm that specializes in handling complex drug and personal injury cases on behalf of clients and injured persons all over the US. The company has provided successful representation in a hip recall lawsuit and hip replacement lawsuit.