St. Jude Heart Valve Lawsuit

By Heidi Turner

Three years after introducing the St. Jude Heart Valve, they were recalled because they were making too many people sick. In some cases, the valve detached from the rest of the heart.

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St Jude Heart Valve Claims

The company is accused of negligence in its research and development of the valve, and purportedly should have known there would be problems with the valve before it sought approval from government regulators. It is also accused of withholding important information from regulatory authorities.

The company is also accused of aggressively marketing the product without proper testing.

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If you or a loved one has suffered personal injury from this heart valve device, you may qualify for damages or remedies that may be awarded in a possible class action lawsuit. Please fill in our form to submit your complaint and we will have a lawyer review your St. Jude complaint.

At LawyersandSettlements.com, it is our goal to keep you informed about important legal cases and settlements. We are dedicated to helping you resolve your legal complaints.

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Last updated on Jan-25-17

ST JUDE HEART VALVE LAWSUITS

Defective St Jude Cardiac Defibrillators Class Action Lawsuit alleging battery depletion defects
Premature Insulation Failure in Recalled St. Jude Medical Riata Defibrillator (ICD) Leads
St. Jude Medical recall for allegedly defective Implantable Cardioverter Defibrillators.

ST JUDE HEART VALVE LEGAL ARTICLES AND INTERVIEWS

The FDA Warning Letter RE: St. Jude ICD Batteries One Year Later

February 10, 2018

Sylmar, CA: We will soon be coming up to the one-year anniversary of the receipt by Abbott Laboratories of a scathing warning letter by the US Food and Drug Administration (FDA). At issue were various allegations and findings of non-compliance and failures to maintain good manufacturing practices determined during an inspection of its facility in Sylmar, California. Of interest to litigants bringing St. Jude ICD and CRT-D device lawsuits, are findings of non-conformity with regard to its cardiac defibrillator line - namely its Fortify, Unify, Assura and Quadra devices. READ MORE

Canadian Class Action Launched Against Defective St. Jude Cardiac Defibrillators

January 13, 2018

Toronto, ON: Imagine the panic one might feel when told the defibrillator relied upon to help keep you alive, could fail at any time and with little warning. In reality, that circumstance is one Canadian lawsuit plaintiff Shirley Houle didn’t have to imagine. Amongst the St. Jude ICD and CRT-D device lawsuits, is a Canadian class action launched this past May. READ MORE

Alaskan Health Insurer Sues Abbott / St. Jude over Defective ICD Batteries

December 24, 2017

Chicago, IL: Chicago may be far removed from Alaska geographically, but Illinois serves as home base for a proposed St. Jude class action lawsuit brought by an Alaskan union-benefits fund against St. Jude manufacturer Abbott Laboratories (Abbott). READ MORE