Tag Archives: Pacemaker Recall

Boston Scientific Accolade Pacemaker Recall Issued Due to Early Failure Risks

December 17, 2024 By: Martha Garcia

High lithium salt concentrations in the recalled pacemaker batteries can lead to a loss of life-saving heart rhythm support.
Ingenio Pacemaker, CRT-P Recall Issued After Dozens of Incidents and Patient Injuries

August 09, 2021 By: Russell Maas
Medtronic InSync III Pacemaker Recall Issued Due to Defective Battery Risk

December 09, 2015 By: Russell Maas
Medtronic Pacemaker Recall: Kappa 600/700/900 and Sigma 100/200/300

June 15, 2009 By: AboutLawsuits
Medtronic Pacemaker Defects Reported Among Kappa and Sigma Devices

May 21, 2009 By: AboutLawsuits

MDL Panel To Consider Depo-Provera Brain Tumor Lawsuit Consolidation at Hearing Today (Posted 5 days ago)

The U.S. JPML will hear oral arguments today over the potential creation of a Depo-Provera brain tumor lawsuit multidistrict litigation, which would place all of the federal cases under one judge for coordinated pretrial proceedings.

Paraquat Lawsuits Over Parkinson’s Disease Risk Set for Trial in October 2025, April 2026 (Posted 6 days ago)

With more than 5,800 Paraquat lawsuits being pursued by individuals who developed Parkinson’s disease following exposure to the herbicide, the early bellwether trials will test allegations that will be repeated throughout the litigation.

Junk Food Lawsuit Over Teenager’s Type 2 Diabetes, Fatty Liver Disease Diagnosis Removed to Federal Court (Posted 7 days ago)

Several junk food manufacturers have removed a recently filed lawsuit to federal court after it was originally filed in Pennsylvania state court, where none of the defendants are based.

Tag Archives: Pacemaker Recall

Boston Scientific Accolade Pacemaker Recall Issued Due to Early Failure Risks

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

Medtronic InSync III Pacemaker Recall Issued Due to Defective Battery Risk

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

Medtronic Pacemaker Defects Reported Among Kappa and Sigma Devices

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