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.
Interested in the Bard PowerPort lawsuit?
Tag Archives: Becton Dickinson
-
-
Bard PowerPort Lawsuit Filed Over Catheter Bloodstream Infection
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.
-
BD Intraosseous Needle Kit Recall Issued Over Risk of Serious Injury or Death
The FDA has announced a class I recall for thousands of BD needle kits and drivers used to access blood vessels in bones.
-
Judge Rejects Motions to Overturn Bard Hernia Mesh Lawsuit Verdict or Hold New Damages Trial
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…
-
New Trial Sought on Bard Hernia Mesh Damages Following $255k Verdict
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…
-
Bard Hernia Mesh Lawsuit Ends in $255K Jury Verdict
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 ChloraPrep Applicator Recall Expanded Nationwide Due To Microbial Contamination Risk
BD is expanding a ChloraPrep applicator recall which may be tained by microbial contamination.
-
Do Not Use ChloraPrep 3 mL Applicators Due to Microbial Contamination Risk, FDA Warns
The FDA is warning against the use of certain BD ChloraPrep applicators due to the risk of microbial contamination and infections.
-
Bard Surgical Mesh Settlement Results in $60M Payment To States
C.R. Bard will pay $60 million to resolve claims with most states that its transvaginal mesh products were deceptively advertised.
-
FDA Says BD Alaris Infusion Pump Problems Could Lead to Severe Injury, Death
The FDA is warning problems with some recalled Becton Dickinson Alaris infusion pumps could cause serious injuries or death.
