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Healthcare Providers Cautioned Against Using Modified Synovo Hip Replacement Systems The U.S. Food and Drug Administration (FDA) has recently issued a crucial warning to healthcare professionals regarding the usage of the Total Hip System, including its implants manufactured by Synovo Production, Inc. This advisory comes in the wake of significant modifications made to three […]
Modified Synovo Hip Replacement Lawsuits
The U.S. Food and Drug Administration (FDA) has recently issued a crucial warning to healthcare professionals regarding the usage of the Total Hip System, including its implants manufactured by Synovo Production, Inc. This advisory comes in the wake of significant modifications made to three key components of the system, diverging from the original versions cleared by the FDA. These changes have raised serious concerns about the safety and efficacy of the system and its components, specifically the femoral resurfacing cup, acetabular fixation cup, and acetabular bearing.
The FDA’s alert extends to patients who have received these implants since 2019. The system, also known as the total hip replacement system, Synovo Preserve, and Endotec BP, has been under scrutiny following the discovery of these unauthorized alterations. In 2022, after detecting the modifications, the FDA conducted an inspection leading to a warning letter issued to Synovo. This letter highlighted multiple violations and demanded an immediate halt in the production of the modified devices, along with a correction of the noted violations. The FDA has also asked Synovo to inform their customers about the risks associated with these devices.
Moving forward, the FDA is working collaboratively with Synovo to ensure compliance with regulatory standards. Meanwhile, the agency strongly advises against the acquisition or use of the currently available Synovo Total Hip System. Healthcare providers are urged to eliminate these systems and any affected implant components from their inventory. Additionally, the FDA recommends vigilant monitoring of patients who have been fitted with the Synovo system, for signs of potential complications such as bone loss, device loosening, or wear and failure.
Patients who have suffered harm due to the modified Synovo hip replacements may have legal grounds to seek compensation through product liability lawsuits. These legal actions are designed to hold manufacturers accountable for injuries caused by their products, particularly when safety standards are not met or when there is a failure to inform about potential risks.
Filing a product liability lawsuit involves a series of steps, starting with the establishment of the claim. For patients impacted by the Synovo hip replacements, this would involve proving that their injuries or complications are directly linked to the use of these modified devices. Collecting medical evidence, expert opinions, and other relevant documentation is crucial in building a strong case.
Given the complexity of such cases, especially when confronting large manufacturers, the assistance of an experienced attorney becomes invaluable. A skilled lawyer can guide clients through the legal process, handle negotiations, and, if necessary, represent their interests in court. An attorney’s expertise is crucial in overcoming the legal hurdles and in ensuring that the victim’s rights are adequately protected.
Victims of the faulty Synovo hip replacements could be entitled to various forms of compensation, including medical expenses, lost income, and damages for pain and suffering. In some cases, punitive damages may also be pursued, particularly if the manufacturer’s negligence is evident.
Free Consultation for Those Impacted by Synovo Hip Replacement Issues
For individuals affected by the Synovo hip replacement complications, it is important to take prompt action. Parker Waichman LLP, a national law firm specializing in product injury cases, provides critical support and guidance. Offering free consultations, they assist victims in understanding their legal options and the steps involved in pursuing a claim.
Victims can contact Parker Waichman LLP at 1-800-YOUR-LAWYER (1-800-968-7529) to initiate the process of seeking justice and compensation. With their expertise in product liability cases, Parker Waichman LLP is committed to helping those adversely affected by these medical device issues.
Regardless of your location or where your injury occurred, our nationwide personal injury law firm is ready to assist you.