Did you have a Hip Replacement?

The FDA has recalled some Metal-on-Metal Hip Replacements. You may be able to file a claim against the manufacturer.

Call 1-800-288-2886 or e-mail us today.

NBC News Reports on “Nation’s Largest Medical Device Failures Ever”

NBC Nightly News reported on October 4, 2011:

“One type of replacement hips that’s been installed over the years is starting to fail leaving doctors and patients facing one of this nation’s largest medical device failures ever.”

See the full video report  by clicking here.

New York Times: Metal Hips Failing Fast, Report Says

Published September 15, 2011: “In a troubling development for people with all-metal artificial hips, a registry that tracks orthopedic implants in Britain reported on Thursday that the failure rate of the devices was increasing. The National Joint Registry for England and Wales said that an all-metal artificial hip once sold by Johnson & Johnson had failed in an estimated one-third of the patients who had been followed for the longest time. The device was recalled by the company last year. The British registry also found that the early failure rate of some other “metal-on-metal” hips — ones in which both the ball and the socket components of an artificial joint are made of metal — was significantly higher than for those made from other materials, including a combination of metal and plastic. While the patients tracked by the British registry are not in the United States, doctors and patients here pay close attention to the registry’s findings because no such body exists in this country, where there is far greater use of artificial hips and knees. Australia also keeps a registry. There was already heightened concern in the United States about the all-metal hips. In the first six months of this year, the Food and Drug Administration received more reports about problems with the all-metal hips than it had in the previous four years combined, according to an analysis by The New York Times. In May, the F.D.A. took the unusual step of ordering producers of the devices to study how frequently they were failing and to examine the health implications for patients.”


Read the entire article by clicking here.


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