Showing posts with label Hip Implants. Show all posts
Showing posts with label Hip Implants. Show all posts

Monday, March 21, 2016

J&J/Depuy Hip Replacement Verdict: Pay $502 Million To 5 Plaintiffs (of More Than 7000 Nationwide) In Texas

lawyersandsettlements

March 18th, 2016. By 

Top Settlements

Hip-Hip-Hooray! Well, sort of–though it probably doesn’t go far enough to take away all that the victims have been through. But here’s a whopper. To the tune of $502 million. That’s the verdict awarded to five plaintiffs in a bellwether trial concerning Johnson & Johnson’s DePuy Pinnacle metal-on-metal hip replacement devices.
The math goes $142 million in compensatory and $360 million punitive damages. The verdict was reached following 37 days of testimony in the US District Court for the Northern District of Texas Dallas Division.
The trial consolidated cases involving five separate plaintiffs who are residents of Texas. The lawsuits, including those of more than 7,000 plaintiffs nationwide in the multidistrict litigation (MDL), claim that the DePuy implants were defective and caused metal debris to enter into patients’ bloodstreams, causing severe injuries and sometimes leading to revision surgery.
According to attorneys for the plaintiffs, the evidence in the testimony against J&J was ground breaking, particularly in relation to what, in effect, amounted to hundreds of millions of dollars in bribes to orthopedic surgeons to use and recommend this product.
Plaintiffs’ attorneys also discovered several instances in which physicians lied in medical clinical testing of the devices and forged consent forms for patients who were using the product to lie about the results the patients experienced with the product.
Risperdal Settlement… Ortho-McNeil-Janssen Pharmaceuticals also got hit with a large Risperdal settlement this week—$124 million to be precise, ending nine years of litigation dealing with allegations it illegally promoted the anti-psychotic prescription drug Risperdal for unapproved or “off-label” uses. Ah, that old chestnut.
The charges were brought by South Carolina Attorney General Alan Wilson. In February he announced that Ortho-McNeil-Janssen will pay $124,324,700 in satisfaction of the settlement to South Carolina.
According to the lawsuit, Ortho-McNeil-Janssen employed aggressive marketing techniques to persuade doctors to prescribe the drug to their patients, including children with disabilities and elderly dementia patients. The company sent more than 7,000 letters to doctors, allegedly overstating the efficacy of Risperdal without FDA approval.
Risperdal (generic name Risperidone) is an atypical antipsychotic that works by changing the activity of certain natural substances in the brain. Developed by Janssen Pharmaceuticals, a subsidiary of Johnson & Johnson, Risperdal was approved by the FDA in 1993 for the treatment of schizophrenia in adults. Risperdal side effects include gynecomastia (male breast growth), tardive dyskinesia, high blood sugar and diabetes, stroke, heart attack and even death. As of September 2012 more than 420 Risperdal lawsuits had been filed, 130 of which are gynecomastia claims. 
Ok, that’s a wrap folks…Have a good one. See you at the Bar!

Thank You LucyC and Lawyers and Settlements

pic cred to topclassactions.com

Tuesday, April 16, 2013

J&J Jury Urged To Award $5 Million For Failed Metal Hip

Bloomberg has;
J&J Jury Urged To Award $5 Million For Failed Metal Hip
By Andrew Harris & David Voreacos - Apr 15, 2013 7:01 PM ET


Johnson & Johnson (JNJ)’s DePuy unit defectively designed a metal-on-metal hip implant and should award an Illinois nurse at least $5 million for harm caused by her device’s failure, her lawyer argued to a Chicago jury.
DePuy knowingly sold defective ASR hips before J&J, the world’s largest seller of health-care products, recalled all 93,000 of the metal-on-metal implants in August 2010, said Denman Heard, an attorney for Carol Strum, the plaintiff. Heard also urged jurors to award extra damages to punish the company.
“Shame on DePuy for allowing this to happen,” Heard said in his two-hour closing argument at a trial that began on March 11. “They could have saved and prevented so much harm.”


Continue reading Bloomberg coverage here.

Thank You Bloomberg, Mr Harris and Mr Voreacos

Tuesday, February 19, 2013

J&J Warns of Safety Risk For 7,500 Non-US Hip Implants

Bloomberg has;
J&J Warns of Safety Risk For 7,500 Non-US Hip Implants
By Shannon Pettypiece & Michelle Fay Cortez - Feb 15, 2013 12:01 AM ET

Johnson & Johnson, the largest seller of health-care products, alerted doctors outside the U.S. to stop using the company’s Adept hip implant after a higher- than-expected failure rate.
A U.K. database found that 12 percent of patients needed a repeat surgery to fix the implant, which hasn’t been sold since 2011, the New Brunswick, New Jersey-based company said yesterday in a statement. About 7,500 of the hips were distributed in 21 countries, not including the U.S. Doctors were sent a safety notice on Jan. 14 about the product.
J&J recalled 93,000 of its ASR model hips in August 2010 and faces 10,000 lawsuits related to the products. The patients that are suing claim the implant left them in pain or immobilized by joint dislocations, infections and bone fractures. They also complain of high levels of cobalt and chromium ions from wear on the devices, in which a metal ball placed atop the femur rotates in a cup implanted in the hip.
J&J acquired the Adept implant in 2009 from closely held U.K. device maker Finsbury Orthopaedics Ltd. J&J said patients who received the Adept devices should be followed according to local standards of care.
Both recalled hip models have the metal-on-metal surfaces.
To contact the reporters on this story: Shannon Pettypiece in New York atspettypiece@bloomberg.net; Michelle Fay Cortez in Minneapolis at mcortez@bloomberg.net
To contact the editor responsible for this story: Reg Gale at rgale5@bloomberg.net

Wednesday, January 30, 2013

Witness: J&J Lowered Own Standards To Deem Metal Hips 'Safe'


Fierce Medical Devices has;
Witness: J&J Lowered Own Standards To Deem Metal Hips 'Safe'
January 29, 2013 | By 

When Johnson & Johnson's ($JNJ) metal-on-metal hip implants failed an internal safety test, the company opted against fixing the issue and instead just changed its protocols, a witness testified in one of thousands of lawsuits the drug and device giant now faces.

As Bloomberg reports, a biomedical engineer told the court that J&J had ample opportunity to fix problems with its now-recalled ASR hip implants, and another witness testified that the device had a 44% failure rate over 7 years, citing Australian data.

J&J has already spent about $900 million to argue and settle suits since the ASR's 2010 recall, but analysts expect the 10,000 lawsuits now pending could cost the company billions.

And this week's testimonies did little to quell the bad press around the issue. Magnus Flett, who led the ASR design team, told the court that the company decided not to redesign the implant for financial reasons, Bloomberg reports, and J&J didn't tell surgeons that ASR failed nearly 8 times as often as other devices because "I don't believe that was clinically relevant."

The plaintiff in the case claims that his ASR implants failed to spur bone growth and abraded to deposit dangerous cobalt and chromium into his bloodstream. J&J contends that it followed procedure in getting FDA clearance for the tech, which the company maintains was not defective.

Meanwhile, J&J is dealing with mounting litigation over Pinnacle, its other, not-recalled metal hip implant. That device is said to fail at a rate of about 10%, which, while below the ASR, still exceeds what's commonly accepted by manufacturers.

And Johnson & Johnson isn't the only devicemaker facing all-metal-hip fallout. Stryker ($SYK) spent about $133 million to deal with its implant recall last quarter, and the company says the whole fiasco could cost $390 million before it's resolved.

None of this has escaped the notice of the FDA, which is proposing a sweeping change in its all-metal hip regulations, requiring manufacturers to prove the safety of their commercialized implants or have them yanked from the market.

- read the Bloomberg report

Related Articles:
Report: J&J knew of hip failure years before recall
FDA wants feedback on tighter hip-implant regs
J&J back in court over DePuy hip implants


Thank You Fierce Medical Devices and Mr Garde



J&J Study Predicted 37% Hip Replacement-Failure Rate

Wednesday, January 23, 2013

J&J Study Predicted 37% Hip Replacement-Failure Rate

Bloomberg has;
J&J Study Predicted 37% Hip-Failure Rate
By David Voreacos & Jef Feeley - Jan 23, 2013 12:01 A


One year after Johnson & Johnson (JNJ) pulled 93,000 metal hip implants from the market, the company internally estimated that 37 percent of the devices would fail within 4.6 years, according to newly unsealed court records.
J&J faces 10,000 lawsuits over its ASR hips, which it pulled in August 2010 after citing U.K. joint registry data showing that more than 12 percent failed within five years. The estimate of triple the failure rate publicly cited by J&J came in documents unsealed Jan. 18 in the lawsuit of Loren Kransky in state court in Los Angeles.
J&J, based in New Brunswick, New Jersey, said in a November filing with the U.S. Securities and Exchange Commission that it increased reserves “due to anticipated product liability litigation and costs associated with” the ASR hips. Photographer: Emile Wamsteker/Bloomberg
Jurors are scheduled to hear opening statements on Jan. 25 in Kransky’s case, the first to go to trial against J&J, the world’s biggest seller of health-care products. J&J offered to pay more than $200,000 a case to settle most of the 10,000 lawsuits, according to five people familiar with the matter. The deal’s cost could exceed $2 billion if most plaintiffs accept the terms. Lawyers for hip recipients have so far rejected the offer, the people said.
The failure-rate estimate came in pretrial testimony of Paul Voorhorst, a biostatistician for J&J’s DePuy unit, which made the hips. A plaintiff’s lawyer, Brian J. Devine, asked Voorhorst about a graph showing the company’s review of 554 implanted hips through September 2011, and how many would fail, requiring follow-up replacement surgery known as revisions.
“That means that 37 percent are expected to fail at 4.57 years, correct?” Devine asked Voorhorst.
“The estimated revision rate at that time would be 37 percent,” Voorhorst said. “That’s correct.”

‘Patient Interests’

Lorie Gawreluk, a DePuy spokeswoman, said that the company was “looking out for patient interests by analyzing data” on the ASR hip system.
She said the analysis cited by Voorhorst “was based on a small, limited set of data that could not be used to generalize the revision rate for ASR, unlike published data from national joint registries that include large numbers of patients and detailed revision information.”
The J&J hips were made from a cobalt and chromium alloy used in two related models -- the ASR XL Acetabular System, and the ASR Hip Resurfacing System. In announcing its recall, J&J cited unpublished data from the U.K. showing that within five years, 13 percent of ASR XL hips failed and needed revision, and 12 percent of the ASR Hip Resurfacing System failed.
In March 2011, the British Orthopaedic Association and the British Hip Society said preliminary data put the ASR XL’s failure rate in the U.K. as high as 49 percent after six years.
Lawyers for patients claim that debris from the metal ball sliding against the metal cup causes tissue death around the joint and may increase the amount of metal ions in the bloodstream to harmful levels. Patients who sued typically cite pain and say they are immobilized by joint dislocations, infections and bone fractures.

Negligent Recall

Claims by Kransky include failure to warn, negligent recall and manufacturing defect.
At the Kransky trial, “DePuy will vigorously defend itself and believes the evidence to be presented will show the company acted appropriately and responsibly,” Gawreluk said.
Kransky, 65, is a retired prison guard who got a hip implant in 2007 and had it replaced in 2012. J&J’s lawyers asked Judge Stephen Czuleger to bar Kransky’s doctors from testifying their patient was “poisoned by the chromium and cobalt” released by the artificial hip, according to publicly filed court documents.
Thomas Trotsky, Kransky’s primary care doctor, said in a deposition that his observations of Kransky over the years led him to conclude that “something was poisoning Mr. Kransky, and, of course, we thought it was the hip,” according to a Jan. 7 court filing.

‘Metal Poisoning’

Trotsky said he and his medical colleagues suspected Kransky was suffering from exposure to “heavy metal poisoning” and they were “unable to identify any other factor besides the prosthetic hip” that could be causing it, according to the documents.
While J&J opposed the motion, the judge ruled Jan. 18 that the doctors can testify. J&J’s lawyers argued that Kransky’s attorneys are seeking to “inflame the jury or appeal to their emotions” by having the doctors testify the former prison guard had been poisoned by the hip’s components.
J&J, based in New Brunswick, New Jersey, said in a November filing with the U.S. Securities and Exchange Commission that it increased reserves “due to anticipated product liability litigation and costs associated with” the ASR hips. The company didn’t specify the amount of the increase.
The company said in January 2012 that it had spent about $800 million on hip recalls during the prior two years. J&J didn’t provide an estimate of its product-liability costs.

10,000 Suits

J&J faced 10,100 suits over the hips through September, according to the November filing. Most pretrial collection of evidence has been consolidated in federal court in Toledo, Ohio, where 7,240 cases are pending, and California state court in San Francisco, where more than 2,000 cases are filed. Other cases have been filed in state courts around the U.S.
In a Jan. 4 court filing, J&J said Kransky has smoked since he was 12, broke his back when he was 15, and was exposed to Agent Orange when he served as a U.S. Air Force mechanic inVietnam. He suffers from diabetes, coronary artery disease, high blood pressure, and kidney disease. He had two strokes and suffers from kidney cancer, according to the company.
Kransky’s case was chosen from those pending in the California Judicial Council Coordinated Proceeding before Judge Richard Kramer in San Francisco.
The Kransky case is Kransky v. DePuy, BC456086, California Superior Court, Los Angeles County (Los Angeles). The consolidated federal case is In re DePuy Orthopedics Inc., ASR Hip Implant Products Liability Litigation, 10-MD-2197, U.S. District Court, Northern District of Ohio (Toledo).
To contact the reporters on this story: Jef Feeley in Wilmington, Delaware, atjfeeley@bloomberg.net; David Voreacos in Newark, New Jersey, at dvoreacos@bloomberg.net
To contact the editor responsible for this story: Michael Hytha at mhytha@bloomberg.net

Thank You Bloomberg, Mr Voreacos and Mr Feeley
HT to Pharmalot