Childers, Schlueter & Smith Newsletter | The Legal Examiner (Page 14)

Cardiac Arrest Caused by Recalled Dialysis Product

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…

By Darren Tobin

/ 4 Oct 2012

Fresenius Medical Care North Fails To Warn of Dangers Posed by Naturalyte GranuFlo

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…

By Darren Tobin

/ 13 Sep 2012

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…

By Darren Tobin

/ 29 Aug 2012

DePuy ASR Hip Implant Settlement Amounts Of First 3 Cases Called Into Question

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…

By M. Brandon Smith

/ 23 Aug 2012

DePuy ASR Hip Implant Settlement Amounts Of First 3 Cases Called Into Question

5th Transvaginal Mesh MDL Formed in West Virginia

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…

By Darren Tobin

/ 20 Aug 2012

Hip Implant Settlements Reached On First DePuy ASR Patients Set For Jury Trial

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…

By M. Brandon Smith

/ 19 Aug 2012

Hip Implant Settlements Reached On First DePuy ASR Patients Set For Jury Trial

Transvaginal Mesh Medical Devices – Thanks to FDA's 510(k) Loophole

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…

By Darren Tobin

/ 3 Aug 2012

Landmark Jury Verdict Takes Down Transvaginal Mesh Manufacturer C.R. Bard Medical

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…

By Darren Tobin

/ 26 Jul 2012

Stryker Recalls Modular Neck Stems Action Specific to Rejuvenate and ABG II Modular-Neck Stems

The FDA announced that one of the world’s leading medical technology companies, Styker, voluntarily recalled its Rejuvenate and ABG II modular-neck stems medical devices. The recall was…

By Darren Tobin

/ 12 Jul 2012

FDA Advisory Panel Meets to Scrutinize the Safety of Metal-On-Metal Hip Implants

Will the FDA issue guidelines in the treatment and monitoring of patients with this device? Many Physicians and patients that our firm have spoken to consistently talk about the lack of…

By M. Brandon Smith

/ 29 Jun 2012

FDA Advisory Panel Meets to Scrutinize the Safety of Metal-On-Metal Hip Implants

Propecia Still Being Given Despite the Known Risks

The hair growth drug, Propecia, was first approved in 1997 by the Food and Drug Administration (FDA). When the drug was first introduced into the market, a number of researchers and doctors…

By Darren Tobin

/ 18 Jun 2012

Johnson & Johnson Chooses to Discontinue Producing the Ethicon Mesh Implants

Ethicon, a subsidiary of Johnson & Johnson sent letters to the judges in federal and state court overseeing vaginal mesh lawsuits to notify them that the company is going to stop selling the…

By Darren Tobin

/ 13 Jun 2012