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 Product Liability

According to court recordsJohnson & Johnson has spent at least $68.7 million to settle hundreds of lawsuits filed by women who suffered blood clots, heart attacks or strokes after using the company’s Ortho Evra birth-control patch.

Majority of users claimed that the patch caused deep-vein thrombosis, (blood clots in the legs), and pulmonary embolisms, (when the blood clots from the legs travel into the lungs). The complaints blamed Ortho Evra for the deaths of 20 women, strokes and heart attacks.

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According to documents filed in federal court, the makers of gadolinium-based contrast agents currently face 391 lawsuits filed by individuals who allege that they developed a rare condition known as NSF, or nephrogenic systemic fibrosis, after an enhanced MRI.

Gadolinium contrast injections are commonly used during MRI and MRA tests to allow doctors to distinguish blood vessels from surrounding tissue by providing enhanced clarity to the images. However, in patients without properly functioning kidneys, side effects of the MRI contrast agents could lead to the hardening and thickening of the skin, which severely restricts movement and could be fatal.

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A Vermont woman was awarded more than $6 million when a jury ordered Wyeth, a pharmaceutical company, to pay her for failing to warn her about the risks of one of its drugs.

But this case was appealed all the way to the US Supreme Court and the Court is set to hear arguments this November.

This case concerns “Federal Pre-emption,” a legal doctrine that can prevent plaintiffs from suing in state court when the products that injured them had met federal standards.

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United States District Judge Rodney W. Sipple issued an order Wednesday designating lawyers in the recently formed NuvaRing birth control MDL to serve in leadership positions and to act on behalf of all plaintiffs during discovery and pretrial proceedings.

On August 22, 2008, the Judicial Panel on Multidistrict Litigation centralized all federal NuvaRing birth control lawsuits in the U.S. District Court for the Eastern District of Missouri before Judge Sipple as part of a federal procedure which allows complex product liability cases to be consolidated and coordinated for pretrial proceedings.

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The FDA earlier this week imposed a ban on 30 drugs made by the Indian pharmaceutical company Ranbaxy Laboratories. Ranbaxy is one of the largest suppliers of generic medicines to the United States.

This ban follows FDA inspections of two of the company’s plants in India that were found to have unacceptable manufacturing controls, no programs to prevent cross contamination, a lack of sterile processing operations and incomplete records. This ban covers generic versions of popular cholesterol drugs, antibiotics and allergy medicines.

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Several thousand MacGregor and Mitre folding soccer goals were recalled today, after the death of a toddler.

The Consumer Product Safety Commission said a 20-month-old Texas toddler was strangled when his head and arm became caught up in the net of one of the recalled goals. The agency received one other report of a child’s head becoming trapped.

The gaps in the recalled nets are about 20 square inches, which is a dangerous size according to the CPSC. The agency says netting should have gaps less than 17 square inches or greater than 28 square inches, to prevent dangerous entanglement and strangulation.

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NHTSA are warning owners of 5 million recalled Ford Motor Co. vehicles to go to dealerships to repair a cruise-control switch system that has been linked to engine fires.

The National Highway Traffic Safety Administration recently issued a second consumer advisory to owners of certain unrepaired Ford, Lincoln and Mercury vehicles that have not responded to previous recalls.

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The FDA in an effort to improve communication with doctors and patients on prescription drug safety, began posting a list of medications under investigation for potential problems.

The list is a compilation naming 20 medications and the potential safety issue for each drug. The listings will be updated for each calendar quarter.

Drugs will be placed on the list based on reports the FDA receives and if FDA safety reviewers determine that a reported problem with a particular drug deserves a closer look, that medication will be on the list.

MARSHALL TEXAS– California resident Canstanza Raspa claims that her development of breast cancer, resulting surgery and mastectomy are the result of 10 years of hormone replacement therapy.

Raspa filed a product liability suit against hormone replacement manufacturers Wyeth, Pfizer, Pharmacia and Upjohn Inc. on Sept 3, in the Marshall Division of the Eastern District of Texas.

The lawsuit alleges that the defendants are liable for claims of fraudulent concealment, negligence, strict products liability, defective marketing, in adequate warnings, negligent misrepresentations, fraud, and breach of express warranty.

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Diabetes patients who use the drug Avandia face an increased risk of serious and potentially fatal injuries of heart attack, stroke, congestive heart failure, bone fractures or death.

Federal lawsuits have been consolidated in an MDL (Multi-District Litigation) in the Eastern District of Pennsylvania.

Avandia is a type 2 diabetes medication which is used to control blood sugar levels. Until 2007, it was one of the best selling medications in the United States, with annual sales in excess of $2 billion.

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