74 results

• Nevro Stimulator Lawsuit MDL Request Opposed by Manufacturer

  August 14, 2026

  Irvin Jackson

  The JPML has been asked to reject a petition by plaintiffs seeking to consolidate all federal Nevro spinal cord stimulator lawsuits before one federal judge, claiming the injuries and claims are too different from plaintiff to plaintiff.

• Abbott Continues to Oppose Spinal Cord Stimulator Lawsuit MDL, Despite Mounting Claims

  August 10, 2026

  Irvin Jackson

  Manufacturer wants the Judicial Panel on Multidistrict Litigation to reject a proposal by a group of plaintiffs to consolidate all federal Abbott spinal cord stimulator lawsuits.

• FreeStyle Libre 3 Class Action Lawsuit Alleges Abbott Sold Defective Glucose Monitors

  July 24, 2026

  Michael Adams

  Three consumers allege Abbott knowingly sold defective FreeStyle Libre 3 glucose monitors that produced dangerously inaccurate low blood sugar readings.

• Nevro SCS Lawsuits Warrant Centralization in New MDL: Motion

  July 8, 2026

  Irvin Jackson

  Plaintiffs have requested that the Judicial Panel on Multidistrict Litigation consolidate all Nevro spinal cord stimulator lawsuits in the Central District of California for pretrial procedures.

• Proclaim Spinal Cord Stimulator Lawsuit Follows Infection, Battery Migration Problems

  July 6, 2026

  Irvin Jackson

  A Texas man's lawsuit claims the electrodes and battery of an Abbott spinal cord stimulator tried to push out of his skin, resulting in a severe infection and the need for surgical removal.

• MDL Sought for Abbott Spinal Cord Stimulator Lawsuits

  June 29, 2026

  Irvin Jackson

  A panel of federal judges has been asked to review a proposal that would consolidate all federally-filed Abbott Laboratories spinal cord stimulator lawsuits before one judge for pretrial proceedings.

• Abbott Spinal Cord Stimulator Battery Problems Led to Repeat Surgeries, Lawsuit Claims

  June 16, 2026

  Michael Adams

  Four plaintiffs allege Abbott spinal cord stimulator battery problems, painful malfunctions and other device failures caused worsening symptoms and repeat surgeries after the company made hundreds of changes to its implant systems.

• Lawsuit Claims Abbott, Boston Scientific SCS Pre-Market Approval Supplements Caused Permanent Injuries

  April 29, 2026

  Michael Adams

  A Florida woman’s lawsuit alleges that Abbott Laboratories and Boston Scientific altered their SCS device batteries, firmware and stimulation features without adequate safety testing approved by the FDA.

• FreeStyle Libre 3 Lawsuits Mount as FDA Issues Class I Glucose Monitor Recall

  February 5, 2026

  Michael Adams

  Federal health officials have issued a Class I recall of certain Abbott FreeStyle Libre 3 and Libre 3 Plus glucose monitor sensors after internal testing found the devices could display dangerously inaccurate low blood sugar readings for extended periods without alerting users.

• FDA Warns 3 Million FreeStyle Libre 3 and Libre 3 Plus Sensors Impacted by Massive Abbott Recall

  January 19, 2026

  Michael Adams

  Federal regulators announced a Class I recall of about 3 million Abbott FreeStyle Libre 3 and Libre 3 Plus sensors, as emerging lawsuits claim the faulty devices triggered unnecessary insulin use and dangerous hypoglycemia after multiple deaths were linked to inaccurate readings.