Lawsuit Alleges Bard PowerPort Failure Led to Deep Vein Thrombosis Injuries
A Bard PowerPort lawsuit claims the drug access port both failed and caused deep vein thrombosis in a patient's neck.
A Bard PowerPort lawsuit claims the drug access port both failed and caused deep vein thrombosis in a patient's neck.
A Bard PowerPort lawsuit claims a defectively designed catheter has led to a woman's catheter bloodstream infection, as well as numerous other complications in other patients.
The FDA has announced a class I recall for thousands of BD needle kits and drivers used to access blood vessels in bones.
The federal judge overseeing all Bard hernia mesh lawsuits has rejected a defense call for a summary motion and plaintiffs' motion for a new damages trial in the wake of…
Plaintiffs awarded $255,000 in a recent Bard hernia mesh bellwether trial are seeking a new trial on damages, saying the jury was wrongly influenced by Court instructions to assign a…
A federal jury awarded a couple $255,000, indicating that the Bard Ventralex hernia mesh had a defective design which led to failure and injuries.
BD is expanding a ChloraPrep applicator recall which may be tained by microbial contamination.
The FDA is warning against the use of certain BD ChloraPrep applicators due to the risk of microbial contamination and infections.
C.R. Bard will pay $60 million to resolve claims with most states that its transvaginal mesh products were deceptively advertised.
The FDA is warning problems with some recalled Becton Dickinson Alaris infusion pumps could cause serious injuries or death.