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 Posted in Personal Injury

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Boston Scientific is exposed to more than 10,000 federal product liability lawsuits filed by women who experienced injuries from transvaginal mesh products implanted for repair of pelvic organ prolapse (POP) or female stress urinary incontinence (SUI).

U.S. federal Judge Joseph R. Goodwin, is presiding over six federal multidistrict litigation for vaginal mesh claims brought against different manufacturers. According to the court, the first bellwether trial involving eleven Boston Scientific cases will begin on October 14, 2014.

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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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Medtronic, Inc., announced that it has agreed to settle 950 of its BMP Infuse Bone Graft product liability injury cases.
Medtronic warned that the initial settlement of $22 million is likely be the tip of the settlement iceberg. The medical device manufacturing giant plans to record a fourth-quarter charge of up to $140 million to cover its initial settlement and the estimated cost of additional settlements.

What is BMP Infuse?

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Wolf Power Morcellator manufacturing company has been sued by a California woman. The woman filed a product liability lawsuit alleging that during a laparoscopic hysterectomy she developed metastatic leiomyosarcoma cancer.
J&J Ethicon Morcellator Cancer AttorneySarah Salem-Robinson and her husband, filed their claim in U.S. District Court for the Northern District of California on May 13, against Richard Wolf Medical Instruments Corporation.

Hysterectomy, Fibroids and Morcellators

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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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Germany based Boehringer Ingelheim, the manufacturer of the anticoagulant medication Pradaxa has agreed to pay $650 million to settle Pradaxa injury lawsuits. There are 4,000 lawsuits on file by folks who allege that the company failed to warn about the risk of severe and deadly bleeding problems with the anticoagulant drug use.

Pradaxa, has been linked to more than 500 patient deaths. The settlement comes about week after the drugmaker  said a new analysis of a company-funded study used to win approval of the Pradaxa found 22 serious bleeding events that weren’t included in the original report.

What is Pradaxa?

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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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Recently, a Texas jury awarded $2.9 million in personal injury damages to a Wise County family that claimed gas extraction wells caused pollution, decreased value of their land and multiple health problems.

fracking water contamination attorneyWhat is Hydraulic Fracturing?

Hydraulic fracturing, also known as hydrofracking or fracking, is the petroleum engineering process for extracting underground natural gas. The Wise County drilling site was in the Barnett Shale, which created a boom in natural gas extraction in the Dallas Fort Worth area, after the explosion of hydraulic fracturing and horizontal drilling techniques.

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Wesley Davis, from New York filed a stroke product liability lawsuit against Actavis and Watson. Davis alleged that the side effects of the testosterone patch AndroDerm caused him to suffer a serious stroke. Furthermore, Davis claimed that the drug manufacturers failed to warn men about the potential risks associated with use of testosterone replacement therapy (TRT).

What is Androderm?

AndroDerm patch is a low testosterone drug approved by the FDA in 1995 for treatment of low testosterone caused by a medical condition, called hypogonadism. The testosterone replacement therapy medication is delivered in permeable skin patches.

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