Bard hernia mesh lawsuits have been filed by individuals who allege that the meshes used to treat hernias were defectively designed, leading to a number of serious complications. Bard is one of the largest manufacturers of hernia mesh in the world, with its products widely used in surgical repair of inguinal and abdominal wall hernias.
HERNIA MESH LAWSUITS AGAINST C. R. BARD
Alleged complications of the hernia mesh injuries include infection, inflammation, organ perforation, pain, fistulas and even death in some cases. Unfortunately, many people who have been injured by these products may not realize that they can take legal action against the manufacturer for their injuries.
It was reported that Bard had up to 60 percent of the global market share for hernia mesh products prior to 2017.
The main Bard Hernia Mesh lawsuits allege that due to defective design, the devices fail and fragment within the patient’s body, leading to a myriad of adverse medical conditions such as chronic pain, infections and the formation of adhesions or scar tissue. Those who have been affected by these defects may be eligible for compensation from Bard or its parent company C. R. Bard Inc., through filing a product liability lawsuit against them.
The basis for these claims rests on whether Bard acted negligently when manufacturing their hernia mesh products—by failing to disclose potential risks associated with their use or when deviating from existing industry standards for safety and quality assurance measures when producing their devices. Additionally, there are theories which assert that certain types of Bard Hernia Mesh Products were dangerously designed or inadequately tested prior to being marketed and sold in mass numbers—both unintended uses which could give rise to a claim against them if proven true in court.
Individuals who have suffered due to defective medical devices like those manufactured by C. R. Bard should speak with an experienced attorney who specializes in product liability litigation. Showard Law Firm can help assess your case and determine whether you may be entitled to damages stemming from your injuries and losses incurred as a result thereof.
FAILURE TO PROVIDE SAFE HERNIA MESH PRODUCTS
The primary complaint among plaintiffs is that Bard failed to adequately warn patients or physicians regarding potential risks associated with Bard hernia mesh products. According to certain reports, Bard was aware as early as 2006 and 2007 that their meshes were prone to failing within a patient’s body yet failed to provide adequate warnings about this issue. Furthermore, according to some lawsuits filed against Bard, they deviated from existing industry standards for safety and quality assurance measures when producing their hernia mesh products.
In addition to infections and inflammation caused by fragments of the hernia mesh device breaking off into the patient’s system, many individuals have experienced other serious complications related to its use. Chronic pain stemming from inflammation has been reported by many who had used Bard’s hernia meshes for repair procedures and it also appears likely that there was an increase in adhesions or scar tissue formed due to the product’s defective design.
Furthermore, serious complications such as organ perforation have also been reported by patients who have undergone treatment using Bard hernia meshes. This is typically caused when pieces of fragmented mesh puncture bodily organs such as intestines or stomach linings and can lead to increased risks for infections or sepsis if left untreated. In some cases however, individuals have even passed away due to complications associated with these devices—a truly alarming circumstance which has highlighted how dangerous these meshes can be in certain situations.
DEVELOPMENTS IN C. R. BARD HERNIA MESH CASES
In recent years, the cases involving C. R. Bard’s hernia mesh products have been gaining more attention as more patients come forward with allegations of injury and death due to their use. As a result, there have been a number of recent developments in the lawsuits filed against the company and its subsidiaries.
One such development is that the FDA has issued a recall on several Bard hernia mesh products due to their potential risks of causing infection and other complications. This recall was one of the first steps taken by the agency to address issues related to these devices, but it is likely only one sign of many future changes coming from the government when it comes to regulating medical devices like hernia meshes.
Another significant development in these cases has been an increase in settlements being offered by C. R. Bard for patients who have experienced adverse effects due to their use of one or more of their products. While this does not necessarily mean that all patients will be able to receive financial compensation for their injuries. Some individuals may be able to obtain monetary damages from these settlements which can help them cover any medical expenses incurred as a result of using the device, as well as provide compensation for any pain and suffering endured due to its use.
ADVOCACY FOR MEDICAL DEVICE REGULATION
Various organizations representing individuals injured by hernia mesh devices are working hard to increase public awareness about this issue and advocate for better regulation of medical devices. There has already been some progress made on this front with new laws being passed in multiple states that require manufacturers to provide more detailed information about potential risks associated with their products before they are sold on the market.
Many attorneys specializing in product liability litigation are continuing to accept cases involving Bard Hernia Mesh injuries and deaths. This could potentially lead to increased legal action taken against C. R. Bard for its negligence in marketing and producing a faulty product leading to harm for unsuspecting consumers. It is clear that there are numerous developments surrounding C. R. Bard’s Hernia Mesh case which have only begun surfacing recently. This could signal bigger changes down the line when it comes to both legally pursuing justice for victims as well as making sure similar occurrences do not take place again in the future due to lax safety regulations.
FILE YOUR CLAIM WITH SHOWARD LAW FIRM
Filing a claim with Showard Law Firm for compensation related to an injury or death due to a defective hernia mesh can be accomplished easily with the help of an experienced attorney. After speaking with our law office, we will need to gather evidence that supports your case, including any medical records and reports related to the injury or death of the affected individual. Once we have obtained this information we will review it and determine if filing a legal claim is feasible.
If so, the next step would be to file a complaint against C. R. Bard in the appropriate court. This complaint should include all relevant details about the incident, including when and how it happened, what type of product was used, any symptoms experienced by the victim, and other pertinent information. These cases are primarily filed either in Rhode Island state court or as part of a Multidistrict litigation based in Federal Court in Ohio.
To date two bellwether cases have been tried and it is expected that a global settlement will be reached in the near future. During this process Showard Law Firm will provide representation for you, our client, throughout each stage of litigation in order to ensure that your rights are protected. You are never required to settle your case in the global settlement and if you are unhappy with the proposed settlement figure you can have your case remanded to the state in which you reside to continue toward trial. At Showard law Firm we will ensure that you are treated as an individual and that you are able to make an informed decision as to the best resolution of your claim.
If you believe you may have been injured by a hernia mesh product contacting Showard Law Firm is essential. Explore potential legal options with us so that justice can be served and you as a victim can receive fair compensation for your injuries and suffering endured due to these defective medical devices manufactured by C. R. Bard.