Williams Kherkher selected among America’s 25 most influential law firms

Williams Kherkher is proud to be included in the list of the America’s 25 most influential law firms for 2016.

This list is compiled by The National Trial Lawyers and was announced in the organization’s magazine, The Trial Lawyer. Members of this list are referred to as “The Forum.” Members of The Forum are nominated by the magazine’s readers. These firms have each demonstrated an ability to make an impact on the practice of law, and have shown leadership, innovation, and success.

Members of The Forum have been invited to a special awards luncheon in South Beach, Miami, on February 6th.

Click here to see the full list.


Former US fentanyl-maker employees arrested

Last month, at six former officials of pharmaceutical company Insys Therapeutics were arrested for allegedly bribing doctors.

According to the court documents, the indicted employees reportedly operated a kickback scheme that motivated doctors to prescribe company’s highly addictive fentanyl product, Subsys. The six ex-employees, including the company’s former CEO, were charged with conspiracy to commit racketeering and wire and mail fraud, and conspiracy to violate the Anti-Kickback Statute.

Initial reports say that the kickback scheme took place sometime between June 2012 and December 2015. Since then, due to company’s aggressive marketing strategies and alleged bribing kickback scheme, the company successfully captured half of the rapid-acting fentanyl products market.

Fentanyl is an FDA-approved synthetic opioid use to manage pain in cancer patients. It is fast acting and 50 to 100 times more powerful than morphine.

If you or someone you love suffered an addiction caused by a fentanyl spray, we might be able to help you. Our lawyers at Williams Kherkher are experienced in litigating pharmaceutical cases and can help you throughout the process. Get in touch with us at (888) 220-0640 to learn more about your legal options.


Impact of FDA power morcellation warning

In 2014, the US Food and Drug Administration (FDA) issued a warning about the potential risks of using laparoscopic power morcellators in hysterectomies or myomectomies. Since the announcement, there was a decrease in the utilization of minimally invasive hysterectomies, based on a retrospective cohort study conducted by the faculty from the University of Michigan Department of Obstetrics and Gynecology.

In the review, the utilization of power morcellators has significantly decreased, but cases in which a practitioner still opts to use major surgical non-transfusion, complications have increased by 27 percent and occurrences of 30-day hospital re-admissions have increased by 25 percent. Although the cause of the shift in practice patterns has yet to be determined, the study suggests that it has something to do with the FDA announcement discouraging the use of the medical device.

If you or someone you know has developed an undetected cancer following a hysterectomy or myomectomy involving a power morcellator, you may be entitled to a financial compensation. Our lawyers at Williams Kherkher have worked closely with these lawsuits and can properly represent you in court. Get in touch with us at (888) 220-0640 to learn more about your legal options.


FDA identifies hospitals non-compliant with medical device reporting standards

At least fifteen hospitals across the United States failed to comply with the medical device reporting requirements, according to the FDA.

The FDA issued a Form FDA 483 to some prominent hospitals, including Massachusetts General Hospital and New York Presbyterian Hospital, for not promptly reporting deaths and injuries related to medical devices pursuant to 21 CFR Part 803. Under the federal regulation, user facilities, such as hospitals and health centers, have only ten days to submit reports about deaths of patients and serious injuries linked to medical devices to its manufacturer and the FDA. The rule also states that a user facility should maintain a medical device event filing system, which can be inspected by FDA. Out of 17 hospitals, 15 medical centers reportedly demonstrated failures to comply with the federal rule following FDA nationwide inspections. The inspection was initiated last December 2015.

If you or your loved one has been physically injured due to an accident involving a power morcellator, you may be entitled to a monetary claim. Our lawyers at Williams Kherkher have the experience and skills to properly represent you in court. Get in touch with us at (888) 220-0640.


Three things you should know about morcellation

A power morcellator is an electronic surgical device that has been used by doctors to minimize how invasive several abdominal procedures can be. However, in 2014, the usage of the device was put under criticism following the announcement of the US Food and Drug Administration (FDA) against the device, citing evidence that morcellators could spread cancer cells throughout a patient’s body. Here are some things you need to know about the device:

  1. Morcellators had been introduced to the public 20 years ago – The US Government Accountability Office (GOA) is investigating the case to determine why FDA cleared morcellators for use despite its potential risks.
  2. Risks of using morcellators are often overlooked – A recent study in South Korea shows that morcellating tumors is more dangerous than removing them with more invasive measures, as this is more likely to spread cancer.
  3. Warning led to changes in surgeries – After the morcellator issue had been spilled into the public sphere, US gynecologists changed the way they perform hysterectomies, preferring other options with fewer complications.

If you have developed cancer following a procedure involving a power morcellator, we might be able to help you. Contact our lawyers from Williams Kherkher at (888) 220-0640.


Williams Kherkher secures $1.5M verdict for client injured in auto accident.

On January 20, 2015 our client broke his leg when he was hit by an SUV while he was attempting to purchase an automobile at an auto auction. The driver of the SUV was a worker sent over by Pacesetter to drive cars at the Manheim Big H auction center. Our client was safely crossing the road when he was struck by a Ford Explorer being driven by the defendant.

Our client was back to work in just 9 months. He turned to Jim Hart and Steve Kherkher to handle his case and handle the case they did.

Steve and Jim spent many long nights strategizing and prepping for trial. After a rigorous trial before Harris County 55th District Court Judge Shadwick, the jury came back with a UNANIMOUS decision in favor of the plaintiff. They awarded the client $750,000 for pain and suffering as well as $750,000 for physical impairment for a whopping total of $1.5 million dollars.

Here at Williams Kherkher, we are so proud of Jim and Steve and the work they put in on behalf of their client and know they will do the same for you or your family members.


Hyland’s stops selling teething products following FDA warning

The U.S. Food and Drug Administration issued a warning about the potential risk of teething tablets and gels to infants and children.

Specifically, the agency urged consumers to temporarily stop using homeopathic tablets and gels after numerous deaths related to the tablets occurred. The products included in the recall were tested by the FDA and found to contain belladonna.

Recently, Hyland’s, a manufacturer of homeopathic teething products, announced it will stop distributing teething tablets and gels in the U.S. following the precautionary warning by the FDA. In a statement released by the company, the manufacturer insisted the products were safe for use because they contained only a tiny amount of belladona, a toxin derived from a poisonous plant. The FDA is urging its consumers to consult with a physician before using any medicine. For a full description of the products included in the recall, you can visit the FDA website.

If your child was affected by Hyland’s homeopathic teething products, we at Williams Kherkher can help you draft a legal case against them. Get in touch with us at (888) 220-0640 to discuss your situation.


FDA urges hospitals to report medical device issues

The US Food and Drug Administration pushes hospitals to streamline their process of reporting problems related to medical devices.

After receiving reports about the potential risk of using hysterectomy surgery devices, the FDA is said to be enhancing the agency’s current reporting system by determining how a medical device causes deaths or injuries. They are also looking at the possibility of forcing all hospitals to submit death and injury reports related to the issue.

The FDA is currently targeting laparoscopic morcellators following the death of a 51-year-old woman who died from uterine cancer. According to reports, the Brigham and Women’s Hospital did not report a case in which a power morcellator reportedly triggered the proliferation of cancer cells in the patient’s body. Meanwhile, the U.S. Government Accountability Office is currently conducting an investigation and will be releasing a report in January.

If you or someone you know has developed cancer after undergoing a surgery involving a power morcellator, get in touch with a lawyer from Williams Kherkher at (888) 220-0640.


Are Power Morcellators Still Relevant in Surgery?

Though the list of side effects in regards to the use of power morcellators tends to grow more and more frightening the longer you look at it, many people claim that the chances of such effects are incredibly low and the question about whether people should use morcellation during surgery lingers.

In the case of Amy Reed, a doctor and opponent to the use of the instrument, had personally undergone uterine fibroid removal three years ago. After her surgery, a rare cancer appeared in her uterine wall and she has since undergone four separate surgeries to remove the subsequent tumors.

Furthermore, the FDA has released a public warning against the use of power morcellators, claiming that they spread the same rare cancer that Reed has faced. The use of the tool has decreased from 13.5% of surgeries calling for them to 2.8%. The number of complications in hysterectomy surgeries has since remained about the same, but the spread of cancer has decreased.

Johnson & Johnson, the largest distributor of the tool, did issue a recall fo their devices, but since it was voluntary, the residual effects have not totally bumped the tool from use. There are several active lawsuits that directly address the morcellator misuse, proving that most people understand that the danger is real.

If you developed previously undetected cancer in the uterine wall following morcellator use, or some other side effect in direct conjunction with the tool, contact one of our attorneys of Williams Kherkher today. Call us at (888) 220-0640 to learn more information.


Williams Kherkher Ranked Among Best Law Firms in U.S. News & World Report

Williams Kherkher has been ranked among the best law firms in Houston and the nation by U.S. News – Best Lawyers “Best Law Firms.” We are honored to have received this prestigious distinction.

Our firm received a Tier 1 rating in Texas and a Tier 2 rating nationally for Mass Tort Litigation and Class Actions for plaintiffs.

The rankings were based on numerous factors, including evaluations from clients, other attorneys in our field, and information provided to the rankings administration. A Tier 1 score indicates that a firm scored within a few percentage points of the highest ranking firm. Williams Kherkher is happy to be included in “Best Law Firms” and we hope to continue doing the work that has earned us our high ratings.

If you have been injured by another person or the negligence of a corporation, call our injury attorneys at (888) 220-0640 to learn about what we can do to help you.


1 2 3 40
SEO for Lawyers