Dialysis Company Failed to Warn of Risks
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...
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...
It is being reported by Harris Martin that the plaintiffs' involved in the first three DePuy ASR Hip Implant settlement cases that were previously set for trial in Nevada are now disputing...
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...
The first ever DePuy ASR hip implant cases set for a jury trial in Nevada has recently settled. It was supposed to be the first courtroom battle in the Counrty of patients with the defective...
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...