On June 27, 2012, the FDA issued a recall for Naturalyte Liquid Acid Concentrate and Naturalyte GranuFlo. These products are made by the Fresenius Medical Care North America Company. Evidence...
The FDA recently issued a Class I recall for Naturalyte GranuFlo and Naturalyte Liquid Acid Concentrate made by the Fresenius Medical Care North America Company on June 27, 2012. The recall was...
A dialysis company failed to warn of the risk their product could cause despite knowledge of the risk. On June 27, 2012, the U.S. Food and Drug Administration (FDA) issued a Class I recall for...
John G. Heyburn II, Chairman for the Panel on Multidistrict Litigation, signed an order that all federal Coloplast transvaginal mesh lawsuits be consolidated for pretrial proceedings as part of a...
It was in 1976 when Congress passed the Medical Devices Amendments defining the required steps for medical device manufacturers to gain the FDA clearance to sell their products. This process is...
A landmark jury verdict makes history for a woman who suffered from the complications of transvaginal mesh. The verdict - $5.5 million dollars – marks a major victory for thousands of women...