Hire An Expert Stryker Recall Lawyer To Get Compensated For Defective Hip & Knee Implants

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.

Improper transvaginal mesh surgery Contact an attorney.

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.