90 results

• Bard PowerPort Wrongful Death Lawsuit Filed Over Device Fractures, Failure

  May 24, 2023

  Irvin Jackson

  A California man has filed a wrongful death lawsuit against the makers of the Bard PowerPort, saying its failure led to the subsequent death of his wife.

• Bard Port Catheter Lawsuit Alleges PowerPort Device is Defective, Unreasonably Dangerous

  May 16, 2023

  Irvin Jackson

  The Bard PowerPort lawsuit claims the defective design of the catheter tube led to a fungal infection and the need for revision surgery.

• Bard PowerPort Infection Lawsuit Alleges Manufacturer Concealed Dangerous Risks

  May 3, 2023

  Irvin Jackson

  A new Bard PowerPort infection lawsuit claims the manufacturer concealed dangerous defects and problems about the device from patients and the medical community.

• Lawsuit Alleges Bard PowerPort Failure Led to Deep Vein Thrombosis Injuries

  March 15, 2023

  Irvin Jackson

  A Bard PowerPort lawsuit claims the drug access port both failed and caused deep vein thrombosis in a patient's neck.

• Bard PowerPort Lawsuit Filed Over Catheter Bloodstream Infection

  March 6, 2023

  Irvin Jackson

  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.

• Arrow MAC Venous Catheter Kit Recall Issued Over Risk of Leaks, Bleeding and Death

  December 19, 2022

  Russell Maas

  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.

• Medtronic Palindrome and Mahurkar Catheter Recall: Defect Could Cause Serious Injury or Death

  August 22, 2022

  Russell Maas

  More than 1 million Medtronic hemodialysis catheters are being recalled due to the risk of leaks which could cause severe injuries or patient deaths.

• Abbott Dragonfly OpStar Catheter Recall Issued Over Tip Separation Risks

  May 31, 2022

  Russell Maas

  A Dragonfly OpStar Imaging Catheter recall was announced after reports of tip separations.

• Medtronic Harmony Delivery Catheter Recall Issued Following Reports of Capsule Breaking

  April 27, 2022

  Russell Maas

  Medtronic is recalling hundreds of Harmony Delivery Catheters due to a risk of separated tips, patient injuries and deaths.

• Medtronic TurboHawk Catheter Recall Issued Due to Tips Breaking

  March 10, 2022

  Randy Dixon, Jr.

  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 injuries.