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A New Jersey Jury has awarded a South Dakota woman $3.35 million dollars in the first vaginal mesh case to go to trial against Johnson & Johnson regarding the Ethicon mesh, reports Reuters.

As reported by the New York Times, Johnson & Johnson/DePuy was aware of massive failures of its ASR metal-on-metal hip replacement system by 2011.

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This information is coming from internal J&J documents as part of a trial expected to begin to today in Los Angeles. The internal analysis showed that nearly 40% of the ASR hips failed within five years of implant. The analysis also suggests that the implant is likely to fail prematurely in thousands of more patients in the next few years. Those patients will have to undergo costly and pain revision surgery.

If you or a loved one have a DePuy ASR hip implant, please call us at 1-800-557-8176 or contact us through our website at hendricksonlaw.com. You may be entitled to a substantial damages award.

For more information on the DePuy implants, see here, here and here.

Johnson & Johnson’s DePuy division may be facing more than $3 billion in damages for its ASR and Pinnacle metal-on-metal hip implants, reports Reuters. Not a surprise to those of us involved in the metal-on-metal implant litigation.

DePuy recalled the ASR metal-on-metal implant in 2010, years after evidence in Europe and Australia showed that these implants were being revised at a rate drastically hirer than traditional ceramic or poly implants. DePuy was forced to recall its ASR implants here in the U.S. after it became clear that a significant percentage of patients with these implants were experiencing metal debris reaction, which included pseudo tumors, infection-like reactions, loss of bone and muscle due to metallosis, early loosening and early failure.

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Shortly after the ASR was recalled, it became clear to many that DePuy’s Pinnacle line was having similar problems. As calls poured in to attorneys around the country regarding the recalled ASR, a significant percentage of the calls were for DePuy Pinnacle implants with nearly identical problems.

Multi-district litigation cases are on-going for both the ASR and Pinnacle implants. MDL cases are contemplated regarding other metal-on-metal implants from other manufacturers. In recent weeks, Stryker has issued a recall on its modular stem system, the first non-bearing surface recall. (The DePuy and Pinnacle cases involve the weight-bearing implant surfaces, namely the artificial ball and cup joint that replaces the natural hip mechanism–Stryker’s implant is a modular femoral stem system that appears to be causing similar reactions as the bearing surface metal-on-metal implants, but due to corrosion at the connection of the modular components, rather than wear due to use of the bearing surfaces.) You can read about the Stryker recall here.

It is clear that there is trouble brewing for many, if not all, metal-on-metal hip implants. If you have experienced any of the following problems as a result of your metal-on-metal implant, please call our office at 1-800-557-8176:
Early Revision
Loosening
Pseudotumor
Metallosis
Implant Failure
Loss of Surrounding Muscle
Continuing Pain

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The FDA has recalled Bard Surgical mesh distributed by RAM Medical, Inc., a medical product distributor in Wayne, New Jersey.

Surgical mesh is used in hernia and other abdominal surgeries to strengthen or repair defects in the abdominal wall or peritoneum. For example, in repairing an abdominal hernia, a surgeon may use surgical mesh to create a “backing” that will reinforce the repair.

The counterfeit Bard surgical mesh ranges in size from 2″x4″ to 10″x14″. It is not properly sterilized, the edges are not properly finished and the weave is larger. This mesh can cause infection and failures of the repair, necessitating additional surgeries and other complications. The counterfeit mesh was distributed beginning October 21, 2008. You can review the recall notice here.

If you or a loved one had a surgery using mesh after October 21, 2008, and have experienced any infection, pain or other complications, you may have received the recalled mesh. If so, you have legal rights that need to be protected. Please call the Law Office of Todd N. Hendrickson at 314-721-8833, or click here to submit an inquiry.

The New York Times is reporting that Congress will investigate Johnson & Johnson makers of Tylenol and the recalled DePuy ASR hip implants.

Johnson and Johnson has been the subject of intensive scrutiny recently. Among the problems is the recall of its ASR hip implants. Initially, DePuy announced they were retiring the line because of low sales. However, the truth came out that the ASR hip implants were experiencing extremely high failure rates in short periods of time, as much as 10% in the first 2 or 3 years of use. These failures are leading to severe injuries and revision surgery.

If you or someone you know has a DePuy ASR metal-on-metal hip implant, contact our office immediately for a free consultation. Todd N. Hendrickson is an experienced medical malpractice and medical product liability lawyer and can help you evaluate your case. Contact us now.

DePuy, a division of Johnson and Johnson, has issued a recall of its ASR metal-on-metal hip implants. There has been a tremendous push by attorneys across the country to attract patients with ASR hips to file cases on their behalf. Before you respond to one of these advertisements, understand that a goal of many of these attorneys is to gather as many of these cases as possible to prosecute them “in volume.” There may be patients for which this type of representation is appropriate, but it won’t be for everyone.

Patients who have DePuy ASR hip implants will basically fall into three categories: (1) those who have had serious and debilitating injuries as a result of receiving an ASR implant; (2) those who have had or will need a revision surgery but obtain a good result; (3) those who haven’t experienced any problems. If you fall into the first category, you should avoid the “mass tort” lawyers. You need individual attention to your case and an attorney who will focus on your unique injuries. If you fall into the last category, you may be an appropriate client for those who will prosecute these cases as part of a class action or multi-district litigation. If you fall into the second category, you should explore the case in more detail.

If you want personal attention to your case, contact our office for a personal consultation.