Fresenius Sanxin Single Use Syringe Recall Issued Due to Risk of Blood, Heparin Leaks
The FDA warns that the recalled syringes could cause infections, blood loss, increased blood clot risks, embolism and death.
The FDA warns that the recalled syringes could cause infections, blood loss, increased blood clot risks, embolism and death.
Separate from a federal court MDL established earlier this year, plaintiffs estimate there will be more than 500 Bard Power Port lawsuits filed in New Jersey state courts in coming weeks and months.
The judge has asked Bard Port catheter attorneys and defendants to file a joint plan to select bellwether test cases for early trials over claims the PowerPorts are defective, leading to fractures and device failures.
A quarter of U.S. women regularly use NSAIDs like Motrin and Advil, which may increase their risk of blood clots by a factor of 11 when combined with high risk birth control, researchers warn.
A group of nearly 40 attorneys have been proposed to serve in various leadership positions in the MDL, which will take actions that benefit all plaintiffs pursuing a Bard PowerPort lawsuit
Lawyers will meet with the court to discuss the organizational structure for a growing number of Bard port catheter lawsuits being pursued over fractures, blood clots, infections and other complications
Missouri woman indicates that the Bard PowerPort Clearvue failure rate is substantially higher than other port catheters, but information about the risk of complications was concealed by the manufacturer
JPML indicates that common questions of fact raised in complaints pending throughout the federal system justify establishing a Bard Port Lawsuit MDL
Manufacturer has opposed Bard PowerPort lawsuit consolidation in an MDL, saying it has quickly resolved previous claims without the need for coordinated pretrial proceedings.
Lawsuit claims a Bard PowerPort failed and caused a breast cancer patient to suffer a Staph infection and an embolism.