Stryker Hip Lawsuit Loans
Pre Settlement Funding for Plaintiffs Involved in a Hip Recall Lawsuit
After two warnings issued by the Food and Drug Administration (FDA) and an increasing number of people who filed lawsuits against Stryker Howmedica Osteonics, Stryker finally recalled two components for the Trident Hip Replacement last January 2008: the Trident Acetabular PSL Cup and the Trident Hemispherical Cups. Stryker said products are used for the socket portion of the hip implant but the FDA found that these products do not meet appropriate standards of sterility.
The Need for Hip Implants
Hip replacement surgery is a very common orthopedic procedure. This can be performed as a total replacement o a hemi (half) replacement. It involves components of the hip joint and the prosthetic / synthetic implant. People who are candidates for hip replacement surgery typically have one or more of the following conditions:
|• Traumatic arthritis (from serious fractures or injuries that cause damage to the articular cartilage) |
• Rheumatoid arthritis (often hereditary and causes inflammation of the synovial membrane)
Prompted by numerous complaints from patients, the FDA sent a first warning letter to Stryker on March 15, 2007 which cited several violations at the Ireland plant, including failure to meet deadlines about following procedures for testing defective products and documenting risk.
According to the FDA, “This inspection revealed that these devices are adulterated within the meaning of section 501(h) of the Act (21 U.S.C. § 351(h)), in that the methods used in, or the facilities or controls used for, their manufacture, packing, storage, or installation are not in conformity with the Current Good Manufacturing Practice (CGMP) requirements of the Quality System (QS) regulation.”
Stryker Hip Replacement Recall
On November 28, 2007 a second warning letter was sent to Stryker which stated that a range of deficiencies have been detected, including Staphylococcus bacteria, the pathogen that causes staph infections and complaints from patients about squeaking ceramic-to-ceramic hip joints.
Under pressure from the FDA, Stryker issued a recall for two of its hip implant components in January 2008 wherein it stated “As a result of the deviation from internal specifications, the Company is initiating a voluntary recall of Trident PSL and Hemispherical Acetabular Cups manufactured in its Cork facility.”
Stryker Hip Replacement Lawsuit Funding
Numerous product liability lawsuits have been filed against Stryker Corporation in recent years. Despite knowledge of potential defects in their product, they failed to take actions which could have prevented serious and permanent injuries for some of their customers. If you have a pending lawsuit against Stryker and are experiencing financial difficulties, TriMark Legal Funding LLC can help you. We provide risk-free, non-recourse lawsuit advance funding (sometimes called lawsuit settlement loans or presettlement funding) from $500 up to $500,000 on more than 200+ different types of lawsuit, including this one.
With your attorney’s cooperation, you could have cash in your hands in as little to 24 to 48 hours.
Curious to see if your case qualifies? Call us toll-free at 1-877-932-2628 or simply apply online!