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.
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.
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.