On July 6, 2012, Stryker issued a voluntary recall of two artificial hip implants. Lawsuits have been filed claiming the Rejuvenate and ABG II hip implants caused severe injuries, and post-market surveillance data showed that both modular necks are prone to fretting and corrosion, which can lead to metallosis—an adverse tissue reaction caused by build-up of metal debris in the soft tissues of the body. It can cause pain, limited mobility, failure of the hip joint, tumors, and dissolution of the bone.
Thousands of Stryker hip implant lawsuits have been filed throughout the United States.
The hip implant devices aren’t considered metal-on-metal (MoM) devices but have metal-on-metal components. Both devices have metal neck pieces that can, under some conditions, rub against a metal stem, causing metallic debris to come loose.
MoM technology is roughly ten years old and became a popular alternative to other hip implants because they were believed to be superior to earlier versions of artificial joints. MoM hip implants account for nearly one-third of the 250,000 replacements performed each year.
Stryker agreed to a settlement and encourages everyone who received a Rejuvenate Modular or ABG II hip implant to contact their surgeon. Patients uncertain if they have one of the recalled hip implants should contact their surgeon or consult their medical records.
If you or a loved one have been injured due to a recalled Stryker hip implant, you are urged to contact the Indianapolis Defective Medical Devices Attorneys of Wilson Kehoe Winingham. The lawyers at WKW can help you get the compensation you deserve. Call 317.920.6400 or fill out an online contact form for a free, no-obligation case evaluation.
Table of Contents
Let WKW put our experience to work for you. Contact us for your free case evaluation.