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 given the Arrow MAC catheter kit recall a class I designation, meaning it poses a risk of serious injury or death to patients.
More than 1 million Medtronic hemodialysis catheters are being recalled due to the risk of leaks which could cause severe injuries or patient deaths.
A Dragonfly OpStar Imaging Catheter recall was announced after reports of tip separations.
Medtronic is recalling hundreds of Harmony Delivery Catheters due to a risk of separated tips, patient injuries and deaths.
The FDA has given a class I designation to a recall of Medtronic TurboHawk atherectomy systems due to a risk of the catheter tips breaking off and causing life-threatening arterial…
Medtronic is recalling more than 95,000 HawkOne Directional Atherectomy Systems whose catheter tips could break off, putting patients' lives at risk.
The FDA is warning against the use of certain BD ChloraPrep applicators due to the risk of microbial contamination and infections.
A Cook Medical Catheter recall has been given class I status by the FDA following dozens of injuries which occurred when weak bonding sites separated during surgery.