9 results

• Boston Scientific Accolade Pacemaker Recall Issued After Thousands of Injuries: FDA

  May 8, 2026

  Michael Adams

  Federal safety officials have announced a recall of certain Boston Scientific Accolade pacemakers, warning a software defect may impair device reliability and the ability to deliver life-sustaining cardiac therapy.

• Boston Scientific Pacemaker Lawsuit Claims Recalled Device Caused Life-Threatening Situation

  February 25, 2026

  Michael Adams

  A Washington woman has filed a lawsuit after her Boston Scientific pacemaker, which was included in a Class I recall, allegedly malfunctioned and intermittently stopped pacing her heart.

• Accolade Pacemaker Recall Issued by Boston Scientific Due to Life-Threatening Injury Risks

  October 14, 2025

  Darian Hauf

  More than 55,000 Accolade and Accolade Proponent pacemakers are being recalled after federal regulators warned that a battery defect may cause the devices to suddenly enter Safety Mode, putting patients at serious risk.

• Boston Scientific Pacemaker Recall Comes After Hundreds of Injuries, Two Deaths Reported

  February 24, 2025

  Martha Garcia

  The FDA warns that battery problems with recalled Boston Scientific Accolade pacemakers puts patients at serious risk of death, with more than 800 injuries and at least two fatalities reported so far.

• Boston Scientific Accolade Pacemaker Recall Issued Due to Early Failure Risks

  December 17, 2024

  Martha Garcia

  The FDA has issued a safety warning, indicating power problems with certain Boston Scientific pacemakers constitute a recall and a potential danger to implant recipients.

• Ingenio Pacemaker, CRT-P Recall Issued After Dozens of Incidents and Patient Injuries

  August 9, 2021

  Russell Maas

  About 48,000 Boston Scientific Ingenio pacemakers and CRT-Ps are being recalled due to a malfunction which could put them into "safety mode", preventing life-saving corrections to patients' heart rhythm.

• Medtronic InSync III Pacemaker Recall Issued Due to Defective Battery Risk

  December 9, 2015

  Russell Maas

  Following the death of a patient, nearly 100,000 Medtronic InSync pacemakers have been recalled due to battery problems which may prevent them from administering life-saving shocks to the heart.

• 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...