LAWSUITS NEWS & LEGAL INFORMATION
Stryker Hip Replacement Lawsuit
Were you looking for Stryker Triathlon Knee Implant Injury lawsuits?
Lawyers are investigating complaints concerning the Stryker Citation, Stryker Meridian and Stryker Accolade hip replacement devices. The issue is not that the devices themselves are defective, but that when they are arranged in a certain way, they may be more likely to cause metallosis in some patients. Some complaints have been made about pain in the area of the hip replacement devices.
Metallosis is caused when metallic debris comes lose from a hip replacement device and is absorbed by the surrounding tissue. It can cause degradation of the muscles and bone in the area, furthermore, if the debris enters the bloodstream, it can travel throughout the patient's body, causing other illness. Metallosis has been reported in other metal-on-metal hip devices, in some cases causing hip implant failure and requiring revision surgery. There is no link yet to these devices and hip implant failure.
Patients who have pain around the site of their hip implant should first check their surgical records to see which device was implanted to replace their hip. If they have a chromium cobalt head (which would be identified by a code number on the surgical records), a blood test must be done to determine if the patient has metallosis. This cannot be shown on an x-ray or CAT scan. The only way to show metallosis is through a blood test.
Last updated on
FREE STRYKER HIP LAWSUIT EVALUATION
Send your Stryker Hip claim to a lawyer who will review your claim at NO COST or obligation.
GET LEGAL HELP NOW
GET LEGAL HELP NOW
Stryker Citation, Meridian and Accolade
All three hip replacement devices—the Citation, Meridian and Accolade—are actually an assemblage of parts that doctors put together when they perform the implant. There are reportedly a number of options for how the doctor can assemble the devices and, when a certain assemblage is used, metallosis may occur.Metallosis is caused when metallic debris comes lose from a hip replacement device and is absorbed by the surrounding tissue. It can cause degradation of the muscles and bone in the area, furthermore, if the debris enters the bloodstream, it can travel throughout the patient's body, causing other illness. Metallosis has been reported in other metal-on-metal hip devices, in some cases causing hip implant failure and requiring revision surgery. There is no link yet to these devices and hip implant failure.
Stryker Hip Implants
In the cases of the Citation, Meridian and Accolade, surgeons were given an option for how to assemble the devices. If the surgeon used an L-Fit, V-40 Chromium Cobalt head but does not use the ceramic head—which acts as an insulator—between the chromium-cobalt and the cup, the metals come into contact with each other, which attorneys believe can lead to metallosis, releasing cobalt and chromium into the patient's tissues.Patients who have pain around the site of their hip implant should first check their surgical records to see which device was implanted to replace their hip. If they have a chromium cobalt head (which would be identified by a code number on the surgical records), a blood test must be done to determine if the patient has metallosis. This cannot be shown on an x-ray or CAT scan. The only way to show metallosis is through a blood test.
Stryker Hip Replacement Legal Help
If you or a loved one has suffered damages or injuries from a Stryker Hip Replacement, please click the link below and your complaint will be sent to a Stryker Hip Replacement lawyer who may evaluate your claim at no cost or obligation.Last updated on
STRYKER HIP LEGAL ARTICLES AND INTERVIEWS
Houston, We Have a Problem with DePuy ASR Hip Replacement
Attorney: Stryker LFIT V40 Femoral Head "Prone to Catastrophic Dislocation"
Stryker Hip Replacement Lawsuits to Move Forward
February 13, 2018
Southlake, TX: Some DePuy ASR hip replacement patients are having problems finding a surgeon to perform revision surgery. Besides having to deal with a defective medical device, surgeons are in a dilemma and the FDA could have done more to help patients. READ MORE
Attorney: Stryker LFIT V40 Femoral Head "Prone to Catastrophic Dislocation"
October 13, 2016
Dallas, TX: Lawsuits have been filed against the maker of the Stryker LFIT V40 femoral head, alleging patients were harmed by use of the hip implant component. Issues associated with the Stryker LFIT V40 femoral head reportedly result in failure of the device, requiring patients to undergo revision surgery to fix the problem. Dr. Shezad Malik, founder of the Dr. Shezad Malik Law Firm, is investigating potential claims against Stryker. READ MORE
Stryker Hip Replacement Lawsuits to Move Forward
May 3, 2013
Stryker hip replacement lawsuits stemming from the recent recall of Rejuvenate and ABG II Modular-Neck hip stems continue to move forward in New Jersey Superior Court. According to Orders issued by the Court on April 29th, Defendants have consented to the use of long and short form complaints submitted by Plaintiffs’ attorneys last month. (In re Stryker Rejuvenate Hip Stem and the ABG II Modular Hip Stem Litigation, No. 296) READ MORE
READ MORE Defective Hip Implant Settlements and Legal News
READ MORE Drugs/Medical Settlements and Legal News
READ MORE Malpractice Settlements and Legal News
READ MORE Personal Injury Settlements and Legal News
READ MORE Drugs/Medical Settlements and Legal News
READ MORE Malpractice Settlements and Legal News
READ MORE Personal Injury Settlements and Legal News
READER COMMENTS
Janice DeJoseph
on
Anonymous
on
Kansas
on