Dr Shezad Malik Law Firm has offices based in Fort Worth and Dallas and represents people who have suffered catastrophic and serious personal injuries including wrongful death, caused by the negligence or recklessness of others. We specialize in Personal Injury trial litigation and focus our energy and efforts on those we represent.

Articles Tagged with Ethicon

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A federal jury in West Virginia today hammered Johnson and Johnson’s Ethicon subsidiary over its transvaginal mesh device. The jury awarded $3.27 million to Jo Huskey over its defective Gynecare TVT Obturator, or TVT-O, transvaginal mesh device. This is one of 33,000 product liability injury lawsuits that claim Johnson & Johnson’s Ethicon Inc unit sold defective transvaginal mesh devices.

Ethicon_Gynecare_Transvaginal_Mesh_LawsuitsFederal Jury Verdict

After a two-week trial, jurors found Ethicon liable for selling defective mesh devices and failing to warn patients and their doctors that they were at risk from serious side effects including pain, erosion, perforation and infection.

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According to a Massachusetts jury, Boston Scientific’s vaginal-mesh sling was not defectively designed and the company properly warned about its health risks. This verdict marks a second victory for the company in two state trials over the vaginal mesh inserts.

vaginal mesh injury lawyer-thumbJurors in state court in Woburn, Massachusetts, cleared Boston Scientific of any liability for Maria Cardenas’s injuries. Cardenas, had the Boston Scientific’s Obtryx sling implanted to fix urinary incontinence problems. According to Cardenas, the sling caused her pain and she was forced to have it removed surgically.

Transvaginal Mesh and Sling Defects

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Endo Health Solutions Inc., said it will pay about $830 million to settle most transvaginal lawsuits. Thousands of injured women allege that its vaginal-mesh implants eroded, left them incontinent and made sex painful.
https://www.youtube.com/watch?v=0Xvv9cd07G8&feature=player_detailpage

Endo’s American Medical Systems Inc. unit reported that it’s settling about 20,000 law suit product liability injury claims over the medical devices, which include the Perigee, Apogee and Elevate implants. Endo, a medical device company based in Ireland, is still exposed to at least 5,000 injury claims against AMS, including some that have been consolidated for pretrial proceedings in West Virginia.

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Johnson & Johnson and its Ethicon subsidiary are exposed to more than 17,500 Ethicon pelvic mesh lawsuits in the federal court system.
Trans Vaginal Mesh AttorneyThousands of injured women have filed Ethicon Gynecare mesh product liability lawsuits for transvaginal repair, pelvic organ prolapse (POP) and female stress urinary incontinence (SUI) damage symptoms after the mesh surgeries.

The Ethicon Gynecare pelvic mesh and bladder sling products have been under fire for causing severe and debilitating injuries when the mesh erodes through the vagina, causing serious infections and the need for revision surgeries.

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Johnson & Johnson’s Ethicon subsidiary has announced that it will stop selling its power morcellators used for uterine fibroid removal surgery. Medical research has shown that use of the devices during minimally invasive laparoscopic hysterectomy and myomectomy procedures may carry a risk of spreading sarcoma cancer.

Medtronic Infuse BMP attorneyJohnson & Johnson Ethicon: No Recall

The company, which manufactured and sold uterine fibroid surgery morcellators since 1998, has stopped sales, promotion and distributing the medical devices after an April 17 FDA warning. The FDA warned doctors to avoid the devices because of the risk of spreading preexisting uterine sarcomas.

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The U.S. Food and Drug Administration today issued two proposed orders to address the health risks associated with surgical mesh used for transvaginal repair of pelvic organ prolapse (POP). If finalized, the orders would reclassify surgical mesh for transvaginal POP from a moderate-risk device (class II) to a high-risk device (class III) and require manufacturers to submit a premarket approval (PMA) application for the agency to evaluate safety and effectiveness.

What is Pelvic Organ Prolapse?
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According to the FDA, doctors should stop using a procedure performed on thousands of American women a year in the course of hysterectomy uterine surgery, because it increases the risk of spreading cancerous tissue.

toxicThe procedure, power morcellation, cuts uterine tissue into pieces that can be pulled out through the incisions made during laparoscopic surgery. The morcellator devices, have been widely used in laparoscopic operations to remove fibroid tumors from the uterus, or to remove the entire uterus.

Morcellator Devices: No Clinical Trials

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Good news for Transvaginal mesh and sling plaintiffs and it’s more bad news for Johnson and Johnson’s (J&J) Ethicon division in its ongoing vaginal mesh debacle. The company will have to pay out again, in these many cases to go to court over its allegedly defective transvaginal mesh products and urinary incontinence slings.

https://www.youtube.com/watch?v=0Xvv9cd07G8&feature=player_detailpage
Johnson & Johnson, the world’s biggest maker of medical products, was ordered by a Texas jury to pay $1.2 million to a woman who alleged that vaginal-mesh implants to treat incontinence was defectively designed. This was the first verdict against the company over those devices.
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According to confidential sources and a news report in Bloomberg, Coloplast A/S, has agreed to pay about $16 million to settle its transvaginal mesh lawsuits. Injured women who were implanted with the Danish mesh manufacturer’s vaginal-mesh inserts had filed personal injury claims against the company.

The Denmark-based Coloplast agreed in January to resolve about 400 suits over the plastic mesh implants which are designed to support internal organs. The settlement is said to provide an average payment of about $40,000 for each claimant.

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Injured women who have alleged product liability vaginal mesh lawsuits against Johnson & Johnson subsidiary Ethicon, have also filed a motion for sanctions. This motion claims that the manufacturer has destroyed a massive amount of data that was relevant to the litigation. Allegedly Ethicon destroyed or lost hundreds of thousands of important documents that should have been preserved.

Thousands of Ethicon Vaginal Mesh Claims

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