FDA requires Strongest Warning Label on Nausea Drug

On Thursday September 17th the Food and Drug Administration required that the strongest warning label be placed on a nausea drug known as Phenegran. This new warning label is due to the fact that after Diane Levine took this drug through an IV push for migraine related nausea and it then led to infection and gangrene. This caused her to have to have her lower right arm amputated. She sued the drug company Wyeth claiming that the warning label was not sufficient enough to warn against the effects of this drug especially in an IV push. This case made it to the Supreme Court and won Diane 6.7 million dollars. This then led to the FDA requiring this strong warning. This will warn users and medical professionals about the possibility of gangrene and also to let them know that IV drugs should be used in low doses and low concentration. This warning is the FDA’s strongest and is called a “black box” warning. The Court agreed that having the Food and Drug Administration’s approval and new warnings help cut down on medical device lawsuits.

For more information on Food and Drug Administration and  improper warning labels you may visit:

This link.

If you or a loved one have experienced a situation similar to this or have been injured due to a medical device or product, please contact a defective product lawyer right away. They will help you fight for your rights to be heard and get the care you or loved one  deserve.

No Such thing as a "nice bike ride in the park," with Dangerous Bike Chain

On Tuesday September 8th 2009, the U.S. Consumer Product Safety Commission and SRAM of Chicago, IL recalled defective bicycle chains and chain connectors because they can crack while in use and cause a fall hazard to the rider of the defective bicycle. One incident has been reported in the U.S. and three incidents outside of the U.S. with these Powerlock connector links, but no injuries have been reported. The recall is specifically on defective SRAM PowerLock connector links on 10 speed bicycle chains sold individually and on some bicycles as part of the original equipment.

If you may have one of these defective chains, play it safe and stop riding your bike and contact SRAM for a free replacement PowerLock connector link.

If you feel that you may have been injured or your rights have not been protected due to this defective consumer product, contact a defective product attorney right away. They can help you get your voice heard and make sure your rights as a consumer are protected.

For additional information concerning this product you may visit the U.S. Consumer Product Safety Commission and the SRAM website at: http://www. sram.com.

Is Your Computer Chair Really Safe?

Each day millions of people sit down on their computer chair to check their email, have conversations with people and even to do business. We also let our children sit at the computer to play computer games, learn or do homework. We all assume that our trusty computer chair in our home is safe; we never consider that to could possibly injury or harm us.  This assumption is wrong.  Each day, millions of products are recalled because they are unsafe and may cause injury. One of these recent product recalls was on the OfficeMax Office Chairs which was found to cause serious injuries to user because it was a fall hazard.

According to the U.S. Consumer Product Safety Commission the chairs were recalled on September 1, 2009 because the back and base were defective and could break during routine use causing a serious personal injury.  The OfficeMax Company has received thirty-six reports of these chairs bases or backs breaking while in use, resulting in fifteen reported personal injuries including lacerations, muscle strains, contusions, and concussions.

The specific office chairs being recalled are the OfficeMax Task Chairs with the model number OM182 and OM96614. The chairs are also charcoal in color and have plastic arms and a plastic and metal base.

If you have one of these office chairs, you should stop using it right away and go to an OfficeMax location for a full refund or a gift card.

If you have been injured or hurt by a defective product like this office chairs or know someone that may have been, you should contact a defective products lawyer right away. They can help you fight for your consumer product safety rights and be your advocate to make sure your rights are protected the way they should be.

For additional information regarding Consumer Safety Product Recalls you may go to the U.S. Product Safety Commission  located here: http://www.cpsc.gov/cpscpub/prerel/prerelsep09.html  and for additional information concerning this specific product recall you may visit: www.officemax.com

Mininno Law Office: In The News

The following is a letter from John Mininno the Courier Post (South Jersey), published on May 24, 2008:

Businesses one-step closer to legal immunity for defective or deadly products

The current war against the American consumer by Big Business and the Bush Administration has gotten a bit nastier.  Apparently, this team of powerful executives and government officials have circumvented an unfavorable Congress and are now using agencies such as the Food and Drug Administration to create rules that make it virtually impossible to sue a business for a defective or dangerous product.  With these rules in place, large corporations can continue to sell toxic dog food, toothpaste, lead paint toys, contaminated heparin and dangerous drugs such as Vioxx and Trasylol, while making millions at the expense of injured consumers.

To divert attention from their wrongdoing and avoid legal responsibility, these companies and sympathetic government officials have demonized trial lawyers and families who file suit to recover the costs of medical bills and lost wages.  If these people could spend one day in my shoes as a trial lawyer, they would be forced to face the fact that real lives are ruined by their greedy desire to make a buck.  These CEO’s have never sat across the room from an inconsolable family, (the way I do on a daily basis), trying to cope with the loss of their loved one who died after using drug that the manufacturer knew was dangerous, but released it anyway.  They have never met one-on-one with a hardworking father who is now unable to provide for his children after using a defective product on the job that took his limb.

Despite these hardships faced by unsuspecting consumers, billion dollar corporations and governmental agencies are trying very hard to paint themselves as the victims of meritless lawsuits.  Meanwhile, the real victims—namely American consumers—are losing their homes, steady paychecks and quality of life because of someone else’s negligence.

Bearing the responsibility for negligence is just a fact of life.  If a drunk driver negligently gets behind the wheel of car and hurts someone, that person is entitled to sue for his or her medical bills, etc.  If someone slips on my sidewalk because I negligently decide not to shovel my snow, that person has every right to sue my homeowners insurance for his or her injuries.  Why, then, should a large corporation be held to a different standard for releasing a dangerous or defective product on the market?

The bottom line is that these companies should be held responsible for their actions.  Whether it’s a fine for releasing harmful chemicals into the environment or paying medical bills and lost wages of consumers that were injured by their products, corporations should be held to the same standard as everyone else in this country.  If Big Business and the Bush Administration truly want to “curb lawsuits,” then I suggest they step it up a notch and produce better and safer products that are tested and tried before their release to the American public.  Safe and happy consumers have no reason to file a lawsuit.  It’s really just that simple.

Free Legal Advice: Defective Products

TWISTER HAMMERHEAD DUNE BUGGIES RECALLED

Today, the US Consumer Product Safety Commission issued a recall for defective Dune Buggies manufactured by TJ Powers Sports, LLC of Irving, Texas. Consumers were warned to immediately stop using the product until further notice. The defect involves a seatbelt adjustment which may break during impact or stress and poses an injection injury and hazard to both drivers and passengers.  Already, 1 consumer has suffered nerve damage to his right arm as a result of the defect.

The product involved is a Dune Buggy by the trade name “Twister Hammerhead” with model number UM150IIR and model year 2004.  This product was manufactured in China and apparently escaped the safety inspection requirements of most products.  For further information go to this link.

Free Legal Advice: Defective Products

More Defective Products From China Being Recalled

On St. Patricks’day, 2008, Mega Brands Inc. recalled about 2.4 million Chinese-made defective product/toys, because small magnets could fall out and cause personal injury such as internal damage. A week later, the same defective product manufacturer recalled 1 million Magtastik and Magnetix Jr. preschool toys. These toys also contained magnets in the small flexible parts of the animals, vehicles and building sets can detach. Since magnets attract, if more than one magnet is swallowed, the magnets can attach to one another and cause personal injury such as additional intestinal perforations or blockages, which can be fatal. The Consumer Product Safety Commission has received 19 reports of magnets falling out of these toys. In one case a 3-year-old boy needed medical treatment to remove a magnet from his nasal cavity.

Click here for the complete list of defective product recalls.
In order to prevent other defective product personal injuries go to our defective products website.

John R. Mininno, Esq. is a New Jersey and Pennsylvania trial lawyer representing clients in medical malpractice, defective products and other serious injury claims. He also writes about issues concerning children’s safety. His offices are in Collingswood, NJ and Philadelphia, PA.

Fentanyl Patches Recall

In the month of February, Fentanyl prescription patches were recalled for the second time because of a product defect that could cause patients to overdose on the potent drug inside.

Actavis South Atlantic, the manufacturer admitted that several lots of the patches sold nationwide might have a defect. The dosages are 25-microgram-per-hour, 50-microgram-per-hour, 75 microgram-per-hour and 100 microgram-per-hour. The patches have expiration dates of May through August 2009. A contract manufacturer, Corium International Inc., manufactured the patches for Actavis.

Similarly, in January of 2008 Johnson & Johnson and Novartis AG’s Sandoz voluntarily recalled a version of Duragesic that also contains Fentanyl. Again, these manufacturers admitted that certain defects might cause leaks that can lead to fatal overdoses. Those recalled patches, manufactured by Alza Corp. on behald of Sandoz Inc. in the U.S have expiration dates on or before December 2009. The defect is an opening that could result in release of the gel made of the drug Fentanyl inside.

Fentanyl is an opioid-based analgesic. High dosages of Fentanyl can lead to severe cardiac and respiratory arrest especially in the elderly and other chronically ill patients. This patient population uses Fentanyl frequently thus increasing the risk of overdoses and death.

Unfortunately, other than the recall, these manufacturers have provided little else in the way of information as to the dangers associated with these patches. Many patients have no way of knowing whether their patch is defective or harmful. More should be done to warn the elderly and other patients before they are harmed.

If you or a loved one has been harmed by an overdose of Fentanyl after using this patch, you may have a claim for damages. For more information, please go to the New Jersey Medical Malpractice Attorneys page.