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GranuFlo Lawsuits Move Forward, as Bernstein Liebhard LLP Notes Upcoming Conference in Federal GranuFlo Recall Litigation
Date:9/20/2013

afety/listofrecalls/ucm309990.htm" onclick="linkClick(this.href)" rel="nofollow">U.S. Food & Drug Administration (FDA) deemed the notification a Class I GranuFlo recall, a designation that is only granted when a medical product poses a significant risk of serious injury or death. According to the Times, the FDA later launched an investigation of Fresenius Medical Care shortly after learning that the company had issued a memo in November 2011 to its own clinics that warned of the heart risks associated with GranuFlo and NaturaLyte. The agency is trying to determine if Fresenius’ delay in notifying dialysis clinics outside of its network violated any federal regulations.*

Court records indicate that more than 300 GranuFlo lawsuits have been filed in courts throughout the U.S., all of which allege that Fresenius Medical Care failed to provide adequate warnings regarding the use of the products, and assert that the company continued to aggressively market GranuFlo and NaturaLyte even after the company became aware of their dangers. In addition to the federal litigation, GranuFlo lawsuits have also been consolidated at the state level in Massachusetts’ Middlesex County Superior Court. (In re Consolidated Fresenius Cases, No. MICV2013-03400-O)

Dialysis patients who suffered sudden and life-threatening heart problems, including cardiac arrest, heart attacks, stroke, and sudden cardiac death, within 72 hours of a dialysis treatment with GranuFlo or NaturaLyte may be entitled to compensation for their injury-related damages. Click Here to learn how to contact a GranuFlo lawyer at Bernstein Liebhard LLP. For additional information, please call 800-511-5092.

*nytimes.com/2012/06/15/health/fda-investigates-fresenius-for-failure-to-warn-of-risk.html; New York Times, June 14, 2012

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