Hernia Mesh Recall Lawyer & Lawsuit. A number of hernia mesh manufacturers have recalled their defective products after. The Hernia Mesh Patch: A Brief Overview. For individuals who are undergoing hernia repair surgery, the mesh patch is typically used to close the hernia and help heal the tissue. Hernia Patch Lawsuit Update: On January 8, 2008, a Federal Court judge expanded the scope of current hernia patch lawsuits to include all Davol/Bard Marlex/Teflon patches, with or without “memory recoil rings.” As early as. Reports of injuries continue to skyrocket after the Ethicon mesh recall, the J and J unit is preparing to defend more than 1,400 Ethicon mesh lawsuits. Consult product labels and inserts for any indications. Hernia Mesh Recall Lawyer & Lawsuit. For individuals who are undergoing hernia repair surgery, the mesh patch is typically used to close the hernia and help heal the tissue. Mesh patches include a . Unfortunately, a number of these memory recoil rings have broken after being surgically implanted, setting off a number of extremely severe side effects that can require additional medical treatment and even more surgery for the unsuspecting patient. What Side Effects have been linked to Hernia Mesh Patches? Numerous studies have been conducted indicating that the memory- recoil ring which surrounds the mesh patch does indeed have a tendency to break. When this breakage occurs, a number of adverse side effects can result including (but not limited to): Bowel obstruction – Partial or complete blockage in the intestines that does not allow the intestinal contents to pass through normally. Maude adverse event report: ethicon johnson and johnson ethicon prolene mesh ethicon prolene hernia system.Bowel perforation – Occurs when an opening forms in the intestinal wall, and its contents flow into the abdominal cavity. Chronic enteric fistulas – Abnormal connection that forms between two parts of the intestine. This condition has been known to cause extreme abdominal pain. Multiple FDA Recalls. In three separate product recalls dating as far back as 2. C. R. The manufacturers initially sent out a recall, urging doctors to stop using some versions of the Kugel patch because a plastic component imbedded in the hernia patch could possibly break causing various injuries to a patient. Under the Freedom of Information Act, the New York Times recently obtained documents indicating that the manufacturers of the Kugel patch did not accurately report the possible severity of complaints to the FDA.
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