Umbilical Hernia Mesh Lawsuit Filed Over Covidien Symbotex Design Defects
An umbilical hernia repair lawsuit claims design defects with the Covidien Symbotex mesh led to adhesions and the need for revision surgery.
An umbilical hernia repair lawsuit claims design defects with the Covidien Symbotex mesh led to adhesions and the need for revision surgery.
A lawsuit over the failure of a Covidien polyester hernia mesh says its lack of flexibility and susceptibility to failure makes it defectively designed for use in the groin.
A Covidien Parietex lawsuit claims the manufacturer knew about problems with the hernia mesh device but failed to warn patients and the medical community.
A Medtronic HVAD recall warns that a driveline cover may become hard and difficult to remove, potentially delaying critical care for heart transplant patients.
The FDA's new recommendations for recalled Medtronic HVAD systems indicate they should not be removed unless medically necessary.
With nearly 6,000 Covidien hernia mesh lawsuits filed nationwide, defendants are asking a federal judge to order coordination between claims coordinated in Massachusetts state courts and the federal MDL.
Medtronic is suggesting health care professionals use mostly untested and unapproved software in backup controllers to help prevent HVAD restart failures.
The FDA warns of potentially fatal cybersecurity flaws linked to the Medtronic MiniMed 600 Series Insulin Pump System.
The FDA has updated a Medtronic breathing tubes recall to provide recommendations to healthcare professionals.
Three plaintiffs' attorneys have been appointed to interim leadership positions in Covidien hernia mesh litigation.