55 results

• Medtronic Pacemaker Recall: Kappa 600/700/900 and Sigma 100/200/300

  June 15, 2009

  AboutLawsuits

  The FDA has notified patients and cardiologists of a Medtronic pacemaker recall for approximately 21,000 Kappa and Sigma pacemakers due...

• Medtronic Pacemaker Defects Reported Among Kappa and Sigma Devices

  May 21, 2009

  AboutLawsuits

  Approximately 37,000 Medtronic Kappa and Sigma pacemakers could contain a wiring defect, according to an advisory letter Medtronic sent to...

• Medtronic Updates Doctors on Reports of Sprint Fidelis Lead Deaths

  March 16, 2009

  AboutLawsuits

  According to a letter sent to doctors on Friday by Medtronic, Inc., at least 107 deaths have been reportedly linked...

• Medtronic Lawsuit Judge will not Remove Himself From Case

  March 10, 2009

  AboutLawsuits

  U.S. District Judge Richard H. Kyle, who dismissed all federal Medtronic lawsuits filed over the recalled Sprint Fidelis defibrillator lead,...

• Medtronic Sprint Fidelis Lead Fractures Continue to Occur as Lawsuits Remain in Limbo

  February 25, 2009

  AboutLawsuits

  Over 16 months after Medtronic issued a Sprint Fidelis recall for small leads used to connect individuals’ defibrillators to their...