Bard Catheter Warning Issued for Blood Clot Removal Device Following at Least 4 Deaths: FDA
Catheter tip could break off, causing blood vessel injuries that could lead to severe injuries or death.
Catheter tip could break off, causing blood vessel injuries that could lead to severe injuries or death.
Catheters with special coatings fared no better than polyurethane when it came to infection and thrombosis risks.
Lawyers are currently completing discovery in a group of 15 Bard PowerPort lawsuits, which will then be narrowed down to six potential trial cases by mid-April 2025.
Each of the selected lawsuits involve allegations that the Bard PowerPort system was defectively designed, resulting in life-threatening complications for plaintiffs.
Parties have until the end of January 2025 to finish depositions and fact discovery for potential Bard PowerPort lawsuit bellwether trials.
Inari Medical issued an Urgent Medical Device Labeling Correction last month, which the FDA has declared a Class I medical device recall.
As the federal litigation heads into it's 2nd year, the Court has re-appointed a group of Bard PowerPort lawsuit attorneys to continue serving in leadership positions in the consolidated multidistrict litigation (MDL)
Bellwether claims will be prepared for early trials to help gauge how juries may respond to evidence and testimony that will be repeated throughout more than 300 other Bard Power lawsuits currently pending in the federal court system.
Barium sulfate used in the port catheter tubes cause Xcela infections and failures, according to lawsuit filed by an Arizona woman who required surgical removal of the port.
Lawyers for Bard PowerPort plaintiffs and the manufacturers indicate they are working cooperatively to move through the discovery process and to meet a deadline in 2025 to select claims for early bellwether trials.