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GranuFlo Lawsuits Mount in Federal Litigation, as Filings Surpass 2,000, Bernstein Liebhard LLP Reports
Date:8/23/2014

dialysis concentrates even after becoming aware of their potential risks.

On March 29, 2012, Fresenius issued an Urgent Product Notification that warned of GranuFlo and NaturaLyte’s association with metabolic alkalosis, a condition that may be associated with serious heart problems. According to the notice, the two products contained a higher level of an ingredient the body converts to bicarbonate, and needed to be dosed differently than rival dialysis concentrates. Two months later, the U.S. Food & Drug Administration (FDA) granted the notification Class I recall status, its most urgent safety alert.

A New York Times report published in June 2012 indicates that the FDA was also investigating Fresenius Medical Care, after finding that the company knew about hundreds of patient deaths that followed use of GranuFlo and NaturaLyte.*

Individuals who allegedly suffered heart attacks, strokes, or other life-threatening heart events within 72 hours of using GranuFlo and NaturaLyte in dialysis may be entitled to compensation for their injuries. Learn more about lawsuits filed after the GranuFlo recall at Bernstein Liebhard LLP’s website, or the Firm’s Facebook page: https://www.facebook.com/granuflolawsuit. For additional information, and to arrange for a free case review, 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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