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A nonprofit consumer advocacy group has requested that the U.S. Senate launch an investigation into Johnson & Johnson. The group alleges a pattern of “reckless” conduct. The same consumer group, the Corporate Action Network, has also urged the Department of Justice to look into whether Johnson & Johnson knowingly destroyed documents related to more than 12,000 pending lawsuits brought by women impacted by dangerous vaginal mesh products. dangerous-goods-labels-1190894-m.jpg

Boston vaginal mesh lawyers know that lawsuits against Johnson & Johnson related to mesh products have largely resulted in plaintiffs obtaining compensation for losses. Juries are clearly finding in many cases that the company acted wrongfully, and that these actions had real consequences for patients affected by the bad products that Johnson & Johnson sold to the public.
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Bellwether cases in transvaginal mesh litigation are moving forward against American Medical Systems (AMS). A December 12, 2013 pretrial order set the first of four bellwether cases, Serrano v. AMS to start April 7, 2014. The company is currently facing as many as 16,534 lawsuits that have been consolidated into a multidistrict litigation in West Virginia. Additional state law claims are also pending against the company, brought by women experiencing serious problems with vaginal mesh products manufactured by AMS. grungy-money-4-1361620-m.jpg

AMS has put aside millions of dollars to try to resolve the pending vaginal mesh litigation, but it remains to be seen whether the company’s costs will be greater than expected. Victims affected by dangerous AMS products can pursue a claim for compensation with the help of a Boston transvaginal mesh lawyer.
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Covidien is a spinoff of Tyco Healthcare that dates back to 2007. Covidien, like many medical devices manufacturers, has produced and sold transvaginal mesh products to women as a method of treating stress urinary incontinence (SUI) and pelvic organ prolapse (POP). Covidien products including the IVS Tunneller, the Duo, Surgipro Mesh, Parietene Mesh and Pelvicol mesh implants. hospital-room-449234-m.jpg

Unfortunately, the Covidien vaginal mesh products are no safer than those made by other major manufacturers including C.R. Bard, Johnson & Johnson, Boston Scientific and American Medical Systems. As such, Covidien is facing lawsuits from women experiencing complications, and these claims have become part of centralized multidistrict litigation (MDL). Victims who had a Covidien product implanted should speak with a Boston transvaginal mesh lawyer about how they can pursue legal action to obtain compensation with losses.
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Stryker has set aside $133 million in order to defend or settle cases arising from defective hip implant products. Problem products include the Stryker Rejuvenate and the Stryker ABG II. Both products contain metal components, although they are not traditional metal-on-metal hip implant systems. surgery-117629-m.jpg

Unlike most hip replacement products, which have a metal acetabular cup and a metal femoral head, Stryker products have four parts including a femoral stem, metal neck, ball and cup. This creative design does not make Stryker products any safer than other metal-on-metal devices and Stryker faces accusations that the company is responsible for serious damage that patients experienced after hip replacement procedures. Victims affected by Stryker products can pursue their own claim for compensation and should speak with a defective hip implant lawyer in Massachusetts for legal help.
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C.R. Bard has the distinction of having lost the first vaginal mesh implant case that a jury decided in the United States. The company is one of several major manufacturers with thousands of pending lawsuits claiming that design defects in transvaginal mesh products are responsible for causing serious injuries and complications for women. usa-dollar-bills-1431130-m.jpg

Women with C.R. Bard vaginal mesh products should consult with a transvaginal mesh trial attorney for assistance in taking legal action and pursuing a damage claim. C.R. Bard’s pattern of losing cases has continued mostly unabated from the first major claim against the company and it seems clear that juries are generally finding that the company should bear the blame when women experience harm due to vaginal mesh.
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DePuy is one of the leading manufacturers of hip replacement devices, but unfortunately is also the manufacturer with the highest failure rates. DePuy products including the Pinnacle Hip Replacement System and the ASR XL System were both designed for younger people undergoing hip replacements and were both made of all metal-components. or-room-lights-33324-m.jpg

Wright Medical, which controls around two percent of the market for knee and hip resurfacing devices in the U.S., also made a metal-on-metal product that was very similar to the DePuy ASR. The Wright Medical product was called the Conserve Plus, and was part of a larger line of Conserve metal-on-metal hip implants.

Both Wright Medical and DePuy are facing thousands of lawsuits related to these metal-on-metal devices. Patients who had a hip implant and who are now experiencing problems should consult with a defective hip implant lawyer help pursuing a damage claim.
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Spinal implants, like those manufactured by Boston Scientific Corp., Medtronic and St. Jude Medical Inc., are geared toward helping patients cope with chronic back pain or nerve damage. backpain.jpg

But a recent Wall Street Journal report reveals that in far too many cases, patients are emerging from the procedure unable to feel at all. Some suffer from partial paralysis. Others have reported experiencing progressive quadriparesis, which is a gradual weakening of each of the four limbs. Other patients report total paraplegia, and are now confined to a wheelchair.

Boston product liability attorneys
know that while manufacturers are staunchly defending these devices, pointing to the fact that some 50,000 spinal implants are conducted annually, no one is eager to slow down and reevaluate the safety of a product that has become an increasingly lucrative aspect of these firms’ business.
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By February 2013, the Food and Drug Administration had issued 95 post-market study orders to 34 manufacturers of vaginal mesh products designed to treat pelvic organ prolapse and another 13 post-market study orders to seven manufacturers of mini-slings. The FDA was prompted to issue these orders by thousands of women experiencing very serious complications from vaginal mesh. old-rubber-stamp-931446-m.jpg

Many of the women affected by mesh products have had to undergo multiple revision surgeries. Many have also begun to take legal action against major mesh manufacturers including Johnson & Johnson’s Ethicon Division, American Medical Systems, and C.R. Bard. Lawsuits have largely resulted in verdicts or settlements for the plaintiffs, including an Atlantic City case awarding a vaginal mesh patient $11.1 million in damages from Johnson & Johnson as well as a West Virginia case in which the plaintiff received $2 million.
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A new social media campaign, a.k.a. Johnson and Johnson Hurts Women, is blasting the manufacturer for lies that have resulted in serious injuries and harm caused by transvaginal mesh products. The website calls for contributors to demand an investigation against the company and to hold Johnson & Johnson accountable for the reckless conduct that injured thousands of women nationwide. According to the campaign, Johnson and Johnson continues to put profits over safety in the marketing and distribution of transvaginal mesh products.
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Organizers of the website are asking employees to be whistleblowers and for investors to divest. It is also calling for supporters to sign a petition for the Attorney General, Eric Holder. Our Boston transvaginal mesh attorneys are committed to protecting the rights of individuals who have suffered harm because of dangerous or defective products. We are committed to safety and health and urge any women who have suffered from transvaginal mesh injuries to step forward and take action against negligent products manufacturers.
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Without admitting liability or fault, Endo International agreed that it would pay $830 million to resolve litigation brought by women who say they were harmed by the transvaginal mesh devices made by its subsidiary, American Medical Systems.
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Our transvaginal mesh lawyers in Massachusetts recognize this is a significant development, as Endo was one of several large medical devicemakers to be confronted with complaints from tens of thousands of woman who had the devices implanted to treat a range of conditions, including stress urinary incontinence and pelvic organ prolapse.

The $830 million settlement by Endo follows a $55 million settlement by the company last year to resolve an undisclosed number of cases. It’s not clear exactly how may lawsuits this settlement covers, but we know there are about 22,000 pending against both American Medical and Endo as of the end of February. In a statement released shortly after the settlement announcement, Endo representatives indicated that this agreement will cover a “substantial majority” of pending transvaginal mesh litigation against both firms.
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