Statute of Limitations for Filing a St. Jude Heart Valve Lawsuit

Statute of  Limitations for Filing a St. Jude Heart Valve Lawsuit

In 1998 all St. Jude mechanical heart valves were recalled due to serious medical complication caused by the use of defectively designed silzone annuloplasty rings. According to numerous scientific studies conducted over the past two decades the use of the St. Jude heart valve can result in a significantly increased rate of paravalvular leaks leading […]

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Embark Resistance Cord Lawsuit – Class Action Claim Information

Embark Resistance Cord Lawsuit – Class Action Claim Information

Our defective product law firm is currently investigating Embark Resistant Band malfunctions resulting in significant harm to consumers. Injure parties have a right to seek compensation vial legal representation in single party lawsuits or part of class action claims. Significant injuries resulting from the defect in the resistant bands include, damage to the eyes resultign […]

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Britax B-Agile and BOB Motion Baby Stroller Recall Attorney

Britax B-Agile and BOB Motion Baby Stroller Recall Attorney

Our law firm has been receiving¬†inquiries with regards to serious finger injuries caused by Britax manufactured strollers. Traumatic hand and finger amputations have been reported in parents and loved ones who attempt to fold the stroller. As a result the Consumer Product Safety Administration has issues a nationwide recall of the product. If you or […]

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Bodum Starbucks Coffee Press Recalled – Product Liability Lawsuit

Bodum Starbucks Coffee Press Recalled – Product Liability Lawsuit

The Consumer Product Safety Administration and the Bodum USA has announces a recall of Coffee Presses sold Starbucks stores due to a high risk of severe injuries. Common injuries associated with the defect in the Starbucks Coffee presses include, severe burn injuries and lacerations cause by flying glass. According to the recall the glass casing […]

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Benicar Class Action Lawsuit Information

Benicar Class Action Lawsuit Information

FDA to Add Warning for Benicar: According to the Food and Drug Administration enough detailed studies have shown a link to the development of severe spruelike enteropathy to warrant a label change on products containing the active ingredient Olmesartan including Benicar. Our law firm is currently investigating class action and single party lawsuits against the […]

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