US Drug Lawsuit Shares Information On Hernia Mesh Recall Cases

December 27, 2019 – – US Drug Lawsuit, a firm based in Inver Grove Heights, Minnesota, has reached out to the community to share information on what they should do if their hernia mesh has been recalled due to a factory defect. The local attorneys host a blog where they share useful resources on several topics, giving the community the benefit of professional advice that can help them decide whether or not they need to reach out to a lawyer. More information is available here: US Drug Lawsuits – Recall of Hernia Mesh.

Patients who have had a hernia mesh implanted to treat their condition may have received an unfortunate mail over the past few weeks mentioning that their product may need to be returned to the manufacturer and replaced by a brand new one. This is because the FDA has recalled several hernia mesh products due to malfunctions or factory defects that either made them unsafe for use in hernia repairs or greatly compromised their durability. This has left countless hernia patients at a loss, wondering what they need to do to return their product and, more importantly, what actions they can take if their defective product caused injuries or worsened their condition.

In light of this worrying situation that affects a significant portion of the US’ hernia patients, the attorneys at US Drug Lawsuit have decided to explain what can be done if the patient has been directly affected by a defective product. A representative from the firm, states, “Several members of the community have already reached out to us asking what to do, and while none have suffered directly due to these defective products, we wanted to share information on what they can do if this were the case. The truth is that the situation is not too different from any other where you may sustain an injury due to a defective product, and you can follow most of the steps that you would for any other injury caused by a malfunctioning product, even if it has already been recalled.”

The attorneys state that a hernia mesh manufacturer’s liability is not limited even if they recall a product, since the company can still be held accountable for the injuries that their defective products have caused when a patient files a lawsuit. This is due to the fact that recalls are voluntary and done at a medical device company’s discretion, and they will only be issued by the FDA if the evidence of adverse effects is overwhelming. According to the firm, there are several details that those affected by such defective products should take into consideration before filing a lawsuit, though acting promptly and seeking an attorney’s assistance is the best course of action.

“If your hernia mesh is defective, and you have been directly affected by its malfunction, you can file a lawsuit against the manufacturer of the product and possibly receive financial compensation for your injuries,” states a drug lawsuits attorney from the firm. They add that the compensation for these cases usually includes full coverage of the patient’s medical expenses, as well as a replacement of the defective equipment and compensation for any additional losses that were directly caused by injuries related to the product.

In such situations, the steps to move forward with the lawsuit are rather simple, as the office states that patients only need to determine the manufacturer responsible for making their hernia mesh as well as the model of the product. Once these crucial pieces of information have been identified, they should reach out to an attorney, who will help them gather further information to proceed with the lawsuit. This includes the date of the surgery and an approximated date of when they began experiencing any discomfort following their medical procedure.

This is a crucial part of the process, as there is a statute of limitations in place that limits how much time a patient has to file a hernia mesh lawsuit. Ideally, patients should contact an attorney and begin building their lawsuit as soon as possible. Those who have been directly affected by a defective hernia mesh may check out this article from US Drug Lawsuits, or reach out to their attorneys in order to request legal advice.

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For more information about US Drug Lawsuit, contact the company here:

US Drug Lawsuit
Greg McEwen
(651) 224-3833
info@usdruglawsuit.com
US Drug Lawsuit & Product Liability Attorneys
1619, 5850 Blackshire Path
Inver Grove Heights, MN 55076
https://goo.gl/maps/cDtpV8P3H7fbQRuNA

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