Defective Hip News
The US Drug Watchdog is expanding its defective hip implant victims initiative to include not just the recalled DePuy ASR hip implant, but all US citizens, who have what is called a metal-on-metal hip implant, that is now failing.
A couple is suing Johnson & Johnson, alleging their toddler son was killed after taking defective Children's Tylenol from a batch that had been recalled - part of the company's continuing string of recalls of drugs and medical devices.
A Washington state couple is suing Johnson & Johnson, alleging their toddler son was killed after taking defective Children's Tylenol from a batch that had been recalled -- part of the company's continuing string of recalls of drugs and medical devices.
A report, published Tuesday in the British Medical Journal, found that patients who received so-called metal-on-metal implants were more likely to require repeat surgery than those who received traditional implants.
The New York Times reports on grim scenes in hospitals nationwide as a more patients seek to have defective metal-on-metal artificial hips removed and replaced. More than a decade ago, some researchers had warned that the hips shed tiny pieces of metallic debris that posed potential health threats to patients. The warnings were ignored, and now doctors and patients face a growing public health problem as one of the country's biggest medical device failures unfolds.
Michael Stieler and his wife, Darlene, weren't surprised when a notice arrived last September from the company that manufactured his artificial hip, DePuy Orthopaedics: His all-metal hip was being voluntarily recalled because of its early failure rates as well as its potential for shedding high levels of cobalt and chromium into the bloodstream.
Rochester, N.Y. - Seven Rochester area residents have filed a lawsuit in district court against a manufacturer for defective hip implants.
The artificial joint implanted in Lebeda's body had been recalled. Its makers, DePuy Orthopaedics, recalled the ASR Hip System in August because it was wearing out faster than expected in some patients. But Atlanta attorney Richard Schlueter, who's representing about 30 metro Atlantans with the defective hip, said DePuy downplayed side effects that are far more serious.
Smith & Nephew Inc. is being accused of violating Food and Drug Administration regulations when making its hip replacement devices.
A recently recalled artificial hip made by a unit of Johnson & Johnson, designed to last 15 years or more, is failing worldwide at unusually high rates after just a few years.
All pretrial proceedings in federal lawsuits against Johnson & Johnson over recalled devices used in hip-replacement surgery will be overseen by a federal judge in Ohio, a judicial panel decided.
PRAIRIE COUNTY - A Prairie County jury awarded $10.3 million to the family of an Iraq war veteran who was burned while rescuing his wife and two children after a devastating collision on I-40 on July 22, 2008.
Mark Rogers and his family were traveling through Arkansas while on vacation when their car was corralled by several tractor-trailers near mile marker 203 outside Biscoe. One of the rigs ignited, and the fire spread, setting Rogers' car on fire. His was the only door that would open, so the 34 year old escaped and kicked in the windshield to rescue his wife, daughter and son.
In total, six tractor-trailers were involved in the catastrophic accident that left three of the four Rogers family members severely burned.
Jim Wilkes and Brian Reddick represented the Rogers family. Five of the companies settled before the trial for a total of $20.5 million. U.S. Xpress, Inc. denied liability and the case went to trial on Sept. 23, 2010.
Wilkes argued that U.S. Express Inc. driver Charles Daniels was following too closely that day and rear-ended a tractor-trailer owned by Triad Transport Inc., causing it to trap the Rogers family in their burning Pontiac. Daniels failed to maintain appropriate speed and distance, and violated other safety regulations, according to the lawsuit.
It took the Prairie County jury only two hours to deliberate.
At the time of the accident, Mark Rogers was a staff sergeant in the U.S. Army Reserves. He had recently returned from his second tour in Iraq, where he served as a combat engineer. In an ironic twist of fate, Staff Sgt. Rogers was a K-9 handler who searched for explosives in Iraq with the goal of maintaining safe highways.
Wilkes & McHugh, P.A., a law firm with offices from coast to coast, is representing clients affected by the recent recall of a Johnson & Johnson hip replacement implant.
Johnson & Johnson announced last month the recall of two kinds of hip replacement implants - one for traditional replacements, and one for resurfacing procedures.
The DePuy Orthopaedics unit of Johnson & Johnson makes the implants. The company said it made the decision to recall the implants because many patients required a second hip replacement surgery after the devices failed. The recalled products are:
ASR XL Acetabular System, a hip socket used in traditional hip replacement; and DePuy ASR Hip Resurfacing Platform, a partial hip replacement intended to preserve more bone. All components of both products are included in the recall. New data shows that five years after implantation, approximately 13 percent of patients (1 in 8) who had received the ASR total hip replacement needed to have a revision surgery.
The ASR XL Acetabular System was launched worldwide in 2004 and approved for use in the United States in 2005. The ASR Hip Resurfacing System had not yet been approved for use in the United States.
Wilkes & McHugh, P.A. is already representing several clients whose implants have failed. If you know or suspect your hip implant might be a DePuy product, you can contact Wilkes & McHugh for more information by calling 1-800-255-5070 or visiting www.defectivehip.com.
The recall, which was issued Aug. 26, 2010, comes two years after the Food and Drug Administration began receiving complaints about early failure rates of the device. As of March 2010, the FDA had received about 400 complaints, many from patients who had to undergo additional surgery to replace the implants, according to The New York Times.
DePuy had announced late last year that it would begin phasing out the devices because of slow sales. In December, the company voluntarily withdrew the ASR hip replacement implant from the Australian market because of higher-than-expected failure rates, the Times reported.
J&J's DePuy Orthopaedics said it was recalling its ASR XL Acetabular System and ASR Hip Resurfacing System -- both used in hip replacement surgery -- due to the number of patients requiring a second hip replacement procedure, or a revision. Some 93,000 people around the world have the ASR hip implant.
More than two years after the Food and Drug Administration began receiving complaints about the failure of a hip replacement implant made by the DePuy Orthopaedics unit of Johnson & Johnson, the company said Thursday that it was recalling two kinds of hip implants.
