109 results

• 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.

• Medtronic HawkOne Directional Atherectomy System Recall Issued Over Broken Tip Risks

  January 25, 2022

  Irvin Jackson

  Medtronic is recalling more than 95,000 HawkOne Directional Atherectomy Systems whose catheter tips could break off, putting patients' lives at risk.