ATTORNEY ADVERTISING - THE LAW OFFICE OF HAKIMI & SHAHRIARI

​​​(888) 635 - 2250

Nothing on this site should be taken as legal advice for any individual case or situation.  Every claim and potential legal claim must be viewed on its own merits. The information on this website is for general information purposes only. It is not intended to create, and receipt or viewing of this information does not constitute, an attorney-client relationship. Every situation and every client’s legal matter is different and this website is merely meant to provide information to the public. Nor does this website create an attorney-client relationship – such a relationship has not been formed unless a signed fee agreement has been made. If you want legal advice or want to know if you have suffered a legal wrong contact the attorneys at The Law Office of Hakimi & Shahriari at (888) 635 - 2250.

About Stryker Hip Implants


In recent years, Stryker Orthopaedics has manufactured metal-on-metal hip implants that have been at the center of several lawsuits alleging that these parts have not been functioning properly and have caused problems within patients who undergo hip surgery. The Stryker Hip Implant lawsuit involves the V40 femoral head used in the Stryker Accolade.  Additionally, Stryker also manufactured the Rejuvenate and ABG II hip modules, both of which were recalled in 2012.
The issue with the metal-on-metal hip implants is that when the parts rub against each other, they send metal particles into the bloodstream. This then leads to metal poisoning due to the release of cobalt chromium from those metal parts into the bloodstream of the patient. Do to the systemic reactions caused by the metal poisoning within the body, metal-on-metal implants have been the focus of widespread recalls and thousands of lawsuits. Health and regulatory agencies within the United States (such as the U.S. Food and Drug Administration), Canada, and the United Kingdom have urged the medical community and patients to routinely examine the patients who use these parts for hip replacement surgery by closely monitoring their blood for metal poisoning. Despite these warnings, the Stryker Accolade V40 femoral head is still currently on the market and has not yet been recalled. However, in late 2016, Stryker issued warnings to patients and medical professionals as to the potentially dangerous risks of using these implants.

 


If you have had symptoms such as hip, leg, or groin pain, popping, clicking or grinding sounds from the hip, hip joint swelling, or decreased mobility following a Stryker hip implant surgery, you may have a case. Other side effects can cause a reaction to the immune system from metal poisoning, which may be characterized by symptoms such as skin rashes, impaired kidney function, fatigue, a weakened or enlarged heart muscle, infection, headache, depression, cognitive impairment, thyroid issues, or hearing and vision problems.

 It can often be financially, psychologically, and physically devastating for patients to undergo such an invasive and painful surgery, only to find out that the parts used were defective and would require a revision surgery. These hip implant lawsuits can result in compensation for loss of wages (past and future), pain and suffering, medical expenses, hospital bills, attorney and legal fees, and other damages. If you or a loved one have experienced any of these harmful side effects or have had to undergo revision surgery, please contact us immediately to obtain more information.

STRYKER HIP IMPLANTS

Law Office of Hakimi & Shahriari

The Law Office of Hakimi & Shahriari
7080 Hollywood Blvd., Suite 804
Los Angeles, California 90028
Toll-Free: (888) 635 - 2250
Fax: (213) 402 - 2170