Hernia meshes, Lawsuit, and Recall – A cycle of awareness

Hernia repair procedures are one of the most frequently conducted surgeries in the USA. But, many victims have endured multiple complications owing to this device. The blog focuses on spreading awareness on the issue and helping potential patients in taking an informed decision.

Hernia meshes have been known to cause complications among a huge percentage of patients. The Food and Drug Administration (FDA) has issued orders for hernia mesh recall to ensure patient safety. Unsterilized manufacturing and faulty design are the main reasons why the implant has been called back.

The hernia, a small bulge in the abdomen wall caused by protruding tissues of the intestine, has been one of the most commonly reported disorders in the United States today. According to FDA, each year close to 800,000 hernia repair procedures are conducted to fix the complications associated with the disorder.

Why recall orders are issued?

As per the FDA, the medical product can be recalled from the market if it poses serious complications to the patients. Apart from that, packing errors or misleading promotional activities can also lead to a product recall.

In regards to hernia meshes, the organization has issued multiple safety communications to big corporations since 2014. The communication was issued based on the following complications:

•    Pain
•    Hernia recurrence
•    Organ perforation
•    Adhesion
•    Development of Infection

Some of the pharmaceuticals slapped with safety warnings from the FDA include:

1.    C.R. Bard
2.    Ethicon (a subsidiary of Johnson & Johnson)
3.    Atrium Medical

Lawsuits and settlements

Patients, suffering from the injuries caused by the hernia meshes, are suing the manufacturers of the polypropylene meshes for manufacturing, distributing, and selling a faulty product. According to them, the pharmaceuticals deliberately hid the facts regarding the safety and effectiveness of the product. Moreover, polypropylene (a product unfit for human usage) was used in these meshes.

A handful of pharmaceuticals have been facing multidistrict litigations, where the plaintiffs are demanding a huge amount of money as compensation.

Awareness among potential victims

The reports on mesh complications and hernia mesh recall have helped several patients in taking an informed decision. People are looking for options, have started questioning the effectiveness of the product, and are now more aware of its implications.

Are you a victim of a called-off mesh and suffering from the complications of the implant? Then, Bernstein, DeCailly & Marshall, PLLC can help you in getting justice. Their no-cost consultation policy and experience over the area makes them the most suitable match for your case. Visit https://bdmlawyers.com or call 844-875-4747, for more information.