September 7, 2010

DePuy ASR Hip Replacement Recall

By now, you may have already heard about the DePuy ASR Hip Replacement product recall. If you are one of the unfortunate recipients of this defective product, you may be left wondering what to do next.

Within 5 years of receiving a DePuy Hip Resurfacing system, it's reported that 12-13% of patients need to have revision surgery to correct the damage. If you've been experiencing pain, malalignment, infection, dislocation or bone fracture, there's a good chance that you fall within the category of recipients necessitating correctional surgery.

Because the poorly designed piece exhibits a dangerous amount of friction between the two metal components, tiny fragments of chromium and cobalt ions are released into your body's soft tissue.

This can compromise the success of the revision surgery so if your surgeon is concerned about this, they should perform a metal ion test beforehand. By performing an ultrasound or MRI scan, soft tissue damage can be visible.

DePuy has agreed to pay what they consider to be reasonable costs for patient evaluation, treatment, and even revision if necessary. They intend to reimburse patients for their medical bills and out of pocket expenses.

As a Seattle personal injury lawyer my firm has extensive experience with product liability cases and I know that dealing with the manufacturer can be a lengthy, complicated process. That's where the experience of a hip recall attorney fighting on your behalf can be essential to recovering the compensation you deserve.

March 2, 2010

Seattle Toyota Auto Accident Victim's Case Raises Questions

Toyota has recalled more than 8.5 million vehicles over auto product defects – primarily sticky gas pedals, defective floor mats that can slip and jam the accelerator, and brake issues. Based on news reports, outside experts even speculate that electromagnetic interference may have caused several incidents of unintended acceleration in recalled Toyota models. Now, the auto maker is facing a government inquiry over whether it tried to delay or avoid a recall in the first place.

Parents of a Seattle resident are one of many who are asking questions about how and why their son died. According to a KOMO News report, like many injured victims or grieving families, the bereaved parents are wondering whether sudden acceleration caused by a sticky gas pedal in the victim’s Toyota Tundra may have caused the fatal car accident on Oct. 17, 2007. The crash occurred when the pickup truck inexplicably crashed head-on into a tree.

Recently this victim’s parents found out that his Tundra was on the recall list as well. They now rightly believe that had Toyota paid attention to the problem, recalled the vehicles and fixed the defects, their son would have been alive.

Toyota's recall comes too late for those in situations similar to this family’s. It is too little too late for those who have suffered catastrophic injuries potentially as a result of the unintended acceleration problem. It is too late for those drivers who have been sent to prison because their car went out of control and injured or killed someone. Seattle personal injury attorneys understand that there have been several car accident cases nationwide where drivers tried convincing juries that it was not them, but their car that was to blame. But no one believed them. Some of those cases are now being reviewed by local prosecutors in different parts of the country.

Continue reading "Seattle Toyota Auto Accident Victim's Case Raises Questions" »

February 17, 2010

500,000 Defective Cribs Recalled after Infant Deaths

The U.S. Consumer Product Safety Commission (CPSC) is warning consumers about defective cribs, which have been responsible for three infant deaths. According to an Associated Press news report, the federal safety agency is recalling 500,000 drop-side cribs, manufactured by Generation 2 Worldwide and ChildESIGNS. The plastic hardware on these cribs can break and allow the drop side to detach, creating a space where the child can become entrapped and suffocated. Also, the mattress supports in these cribs can break away from the crib frames creating a gap where children can suffocate.

CPSC has received three reports of children who died after getting trapped and being suffocated in these defective cribs. The victims were an 8-month-old boy from Ohio who died in June 2007; a 6-month-old boy from Indiana who suffocated in a crib and died in October 2003; and another 6-month-old boy from Virginia who died in September 2002 after two missing screws allowed the lower drop-side track of his crib to pull away from the headboard post. These cribs were sold at retailers nationwide including Buy Buy Baby, Kmart and Wal-Mart.

Several consumers and Seattle products liability attorneys are aware of the fact that more than 5 million cribs have been recalled over the last few years because of similar defects and hazards. Almost all of these recalled cribs were drop-side cribs. These cribs were recalled because when the drop-sides detached, an entrapment and suffocation hazard was created. Inferior parts and poor quality control have also contributed to these product defects.

Continue reading "500,000 Defective Cribs Recalled after Infant Deaths" »

February 9, 2010

Toyota to Fix Defective Gas Pedals

So far, Toyota has recalled more than 7 million vehicles over faulty gas pedals and floor mats. The auto maker has also stopped production and sales of eight models, including its top-selling Camry and Corolla models. The first Toyota recall was issued last year after an auto accident in California killed a highway patrol officer and three members of his family. The officer was in a loaner Lexus and the defective floor mat in the car allegedly caused the accelerator pedal to become jammed. The car accelerated out of control at 120 mph, crashed, and caused four fatalities.

Toyota officials say they have come up with a fix for the gas pedals, which has been approved by the National Highway Traffic Safety Administration (NHTSA). The problem with the gas pedals was that the pedal mechanism could become worn and harder to depress or it could get stuck in a partially depressed position, thus causing sudden or unintended acceleration.

Toyota engineers have been working to insert a spacer in the pedal mechanism in order to increase the tension in a spring and reduce the risk of the gas pedal sticking or staying down. The auto maker has also come under quite a bit of criticism for failing to act quickly on unexpected acceleration issues related to the faulty floor mats. Federal officials say Toyota has known about the problem with the mats since 2007 and has still done nothing to fix it.

Continue reading "Toyota to Fix Defective Gas Pedals" »

February 4, 2010

Cadmium Contamination: Children's Necklaces Sold at Wal-Mart Recalled

About 55,000 children's necklaces sold at Wal-Mart stores are being recalled because they contain high levels of cadmium, according to a news report in consumeraffairs.com. Cadmium is a toxic metal listed high on the U.S. Centers for Disease Control's (CDC) list of substances most harmful to the environment. Cadmium is toxic when ingested by young children and can cause several adverse health effects including brain, kidney, lung and bone damage.

These defective products, which were manufactured in China, were sold exclusively in Wal-Mart retail stores across the country from November 2009 through January 2010 for about $5. The recalled jewelry is in the shape of a metal crown or frog pendant on a metal link chain necklace in a crown hinged box. If you have one of these necklaces at home, please take it away from your child and return the product to Wal-Mart to obtain a full refund.

Continue reading "Cadmium Contamination: Children's Necklaces Sold at Wal-Mart Recalled" »

January 26, 2010

Defective Cribs Recalled for Fall and Entrapment Hazard

Caramia is issuing a product defect recall for about 1,000 "Diane" drop-side cribs. According to a news report in Consumeraffairs.com, the slats on these recalled cribs' drop side can detach from the top and bottom rails posing fall and entrapment hazards to young children. So far, the company has received 18 reports of the slats detaching. No injuries or fatalities have been reported yet as a result of these product defects.

These cribs were manufactured in Slovenia from September 2002 and June 2004 and sold at Buy Buy Baby and other children's products and mass merchandise stores nationwide. They were sold for between $240 and $370. If you have one of these cribs in your home, preschool or childcare facility, please stop using them and call the company to receive a free replacement drop side.

Continue reading "Defective Cribs Recalled for Fall and Entrapment Hazard" »

January 7, 2010

Auto Recall for Range Rover Vehicles Involves Airbag Defects

Jaguar Land Rover North America is recalling 4,001 Land Rover and Range Rover vehicles because of possible airbag defects, which might prevent the front passenger airbag from deploying in the event of a car accident. According to the National Highway Traffic Safety Administration (NHTSA), these affected 2010 Range Rover models may experience airbag lamp illumination on the instrument cluster. The NHTSA report states: “This warning lamp may clear on each subsequent ignition cycle. The passenger airbag will be disabled when the airbag warning lamp is illuminated as a result of this defect and the passenger airbag warning disable lamp in the overhead console will also illuminate.”

The deployment of the passenger side airbag may fail to occur in case of a car accident. This could cause devastating personal injuries and even death to the passenger. When this recall begins, Land Rover dealers will update the vehicles' restraint control module with the integrated diagnostics system tool with updated software.

Continue reading "Auto Recall for Range Rover Vehicles Involves Airbag Defects" »

December 8, 2009

Perfect Flame Grills Recalled for Product Defects that Pose Fire Hazard

A defective product recall has been issued for more than 600,000 Perfect Flame SLG Series gas grills, which were sold exclusively at Lowe's stores. According to a news report in Consumeraffairs.com, the gas burners on these grills can deteriorate causing irregular flames and the lids of some models can catch fire posing a serious fire and burn injury hazard to users. So far, LG Sourcing has received about 40 reports of fires as a result of this product defect and about 23 lids catching fire. There was also one report of an eye injury that required surgery and 21 incidents of burn injuries to consumers' hands, arms or face.

The recalled grills are the SLG series Perfect Flame brand outdoor propane or natural gas grills, which are painted black or gray metal. The products, which were manufactured in China, were sold at Lowe's retail outlets nationwide between September 2005 through May 2009 for between $200 and $500. Consumers who own these defective grills are asked to stop using the products and contact LG Sourcing to get a free replacement burner and depending on the model, a free replacement lid.

Continue reading "Perfect Flame Grills Recalled for Product Defects that Pose Fire Hazard" »

December 3, 2009

Roast Beef Recall Extends to Washington

As trusting consumers, we expect the food products we buy to be free of any substance or ingredient that may cause us harm, illness, or injury. When a food product’s labeling fails to include an important ingredient that many individuals are allegoric to, such as soy, it may be subject to a recall.

According to a Food Safety and Inspection Service (FSIS) report by the United States Department of Agriculture issued on November 4, 2009, Curly’s Food, Inc., has recalled an estimated 12,181 pounds of roast beef deli products. This recall is due to the deli products being accidentally mislabeled in that they contain an allergen – soy. Apparently, the mislabeling issue was revealed after a product check by Curly’s Food, Inc.

Based on the report, the roast beef deli products were made on October 5 and 12, 2009, and were circulated to retail-type delicatessens and Department of Defense Commissaries in Washington and 14 other U.S. states. The report on the recalled product states the following about the product: “Cases containing two (2) various size weight deli-faced pieces of "Healthy Ones, Medium Cooked Roast Beef, 97% Fat Free, No Fillers, No Artificial Flavors, Lower Sodium" in vacuum packaged bags. Each package bears a use by date of "01/03/2010" or "01/10/2010," a case code of "30900-17856" as well as the establishment number "EST. 15878" inside the USDA mark of inspection.”

Continue reading "Roast Beef Recall Extends to Washington" »

November 25, 2009

Stork Craft Crib Recall Largest In U.S. History

The Consumer Product Safety Commission has announced a recall of potentially dangerous cribs, the largest crib recall in the history of the United States. The CPSC is advising consumers to stop using The Stork Craft drop-down-side crib because it poses a serious strangulation risk to infants. Approximately 2.1 million of the cribs have been sold and are in use.

The move follows the news that 4 infants have died of suffocation after becoming entrapped in the crib’s drop down sides. There have also been at least 110 incidents in the United States and Canada when the drop-down sides of the cribs became detached, which resulted in dozens of babies either becoming entrapped between the side and the crib frame, or falling out of the crib altogether.

Drop down side cribs have a track record for injuring infants. Nearly 5 million cribs have been recalled over the past two years and the CPSC has discussed banning dropdown sides all together. Adding to the danger in this particular case is the fact that parts used to create the cribs are easily broken, missing, or misassembled. For instance, the crib's drop-side could come off its tracks and create a "hazardous gap which can lead to infant entrapment and suffocation."

Stork Craft has released a toll-free number for consumers to call, or to order a free repair kit: (877) 274-0277.

Continue reading "Stork Craft Crib Recall Largest In U.S. History" »

November 19, 2009

Flammable Robes Recalled, Linked to Nine Deaths

The connection between nine deaths and extremely flammable women’s robes has instigated a recall by Blair LLC. According to a kfoxtv.com report, a Consumer Product Safety Commission (CPSC) announcement stated that four additional reports of death linked to the full-length women’s chenille robes have been reported to Blair LLC of Warren, PA since June. Because of this, the company has expanded its recall to incorporate additional products imported from the Pakistani manufacturer. The recall now includes more chenille robes and three other chenille products, all made by A-One Textile & Towel, of Karachi, Pakistan.

What has been quite unnerving to consumers is that these dangerous robes were initially recalled in April by Blair after it discovered that three robes caught fire, including one incident in which a consumer suffered second-degree burns. Considering that the robes fail to meet federal flammability standards, they present great risk of serious burns to anyone who wears the garments while exposed to an open flame, such as a stove in the kitchen. Most of the reported deaths linked to the full-length robes took place when the victims were wearing the robes while cooking. A CPSC spokesman said that the victims were mainly in their 70s and 80s.

Continue reading "Flammable Robes Recalled, Linked to Nine Deaths" »

November 11, 2009

Kirk Bernard's Survival Guide to Handling Foodborne Illness

A recent ArticleBase post by Kirk Bernard discusses the Seattle personal injury attorney’s survival guide to handling foodborne illness. Foodborne illness may result from product liability issues and forms of negligence, such as a food product being contaminated from poor handling during manufacturing or a food product containing E. coli bacteria or any other harmful substance. However, there are several precautions people can implement in their own homes to help prevent foodborne illness. The article addresses five main steps that you must take to keep you and your family safe from foodborne illness.

Learn more about how to protect yourself from foodborne illness by reading the entire article.

October 7, 2009

Johnson & Johnson's Voluntary Recall of Infants' and Children's Liquid Tylenol

A recent komonews.com article reported that the McNeil unit of Johnson & Johnson has issued a voluntary recall of 57 lots of liquid Tylenol products, intended for use on infants and children, due to a plausible bacterial contamination. Many parents are shocked to learn that the reputable company revealed that a B. cepacia bacterium was found in a portion of raw material that went unused in the finished product.

Although no bacteria were discovered in the finished product that reached consumers, Johnson & Johnson decided to recall the products as a precautionary measure after consulting with the Food and Drug Administration. As skilled Seattle product liability attorneys, we believe it is better to be safe than sorry in instances such as these, especially when the lives of infants and young children are involved.

According to the report, the recalled products were manufactured between April and June and are made-up of almost two dozen varieties that include Infants’ Tylenol Grape Suspension Drops ¼ oz., Children’s Tylenol Suspension 4 oz. Grape, and Children’s Tylenol Plus Cold/Allergy 4 oz. Bubble Gum. Despite there being a very slim chance that any medical events will take place since the bacterium was not present in the finished products, the company released the following statement: "It was decided, as a precaution, to recall all product that utilized any of the raw material manufactured at the same time as the raw material that tested positive for the bacteria.”

Continue reading "Johnson & Johnson's Voluntary Recall of Infants' and Children's Liquid Tylenol" »

May 2, 2009

Liver Damage and Death Lead to Hydroxycut Recall

Weight Loss Supplement Hydroxycut Recalled Due to Liver Damage, Injuries and Death

Hydroxycut, the number one weight loss supplement in the world, was recalled on May 1st by the FDA. The FDA reports that there are at least 23 reports of serious liver injuries and death (http://www.fda.gov/bbs/topics/NEWS/2009/NEW02006.html), including jaundice and elevated liver enzymes, an indicator of potential liver injury, to liver damage requiring liver transplant. Other health problems reported include seizures; cardiovascular disorders; and rhabdomyolysis, a serious type of muscle damage that can lead to other serious health problems such as kidney failure.

If you or anyone you know have been using Hydroxycut, stop using it immediately. Symptoms to watch for include jaundice (yellowing of the skin or whites of the eyes), brown urine, light-colored stools, fatigue, stomach cramps or pain, weakness, nausea, and vomiting.

This Hydroxycut recall applies to the following products, which are being removed from the market:
• Hydroxycut Regular Rapid Release Caplets
• Hydroxycut Caffeine-Free Rapid Release Caplets
• Hydroxycut Hardcore Liquid Caplets
• Hydroxycut Max Liquid Caplets
• Hydroxycut Regular Drink Packets
• Hydroxycut Caffeine-Free Drink Packets
• Hydroxycut Hardcore Drink Packets (Ignition Stix)
• Hydroxycut Max Drink Packets
• Hydroxycut Liquid Shots
• Hydroxycut Hardcore RTDs (Ready-to-Drink)
• Hydroxycut Max Aqua Shed
• Hydroxycut 24
• Hydroxycut Carb Control
• Hydroxycut Natural

If you have any symptoms of liver injury you should see your doctor immediately. Keep any unused portions of the product for evidence in case you decide to pursue a claim for compensation.

If you have suffered any of these symptoms or injuries contact our experienced Product Defect and Personal Injury Lawyers and click here to visit our website for more information.

November 11, 2007

Recall - “Date Rape” Drug Found in Chinese-Made Toys

Millions of toys made in China have been recalled from North American and Australian shelves. It was discovered by scientists that these toys contain a chemical that converts into a powerful “date rape” drug if swallowed.

Five children, including two in the United States and three in Australia, required hospitalization after ingesting Aqua Dots, a very popular holiday toy distributed by Spin Master Toys. Spin Master Toys is based in Toronto. In Australia, the Aqua Dots are called Bindeez, and were named toy of the year at an industry event earlier this year. Both Aqua Dots and Bindeez are sold by Australia-based Moose Enterprises.

The toy beads are sold on websites and in stores for use in craft projects. They can be arranged in designs and, when sprayed with water, they fuse together.

According to king5.com, scientists say that if the chemical coating on the beads is accidentally ingested, it can turn into the so-called date rape drug gamma hydroxyl butyrate (GHB). Symptoms of poisoning from this compound can include drowsiness, seizures, unconsciousness, coma, and death. GHB is made from common and easily available ingredients.

According to Scott Wolfson, Consumer Product Safety Commission spokesman, the two U.S. children who swallowed Aqua Dot beads went into non-responsive comas.

If you or someone you know has purchased Aqua Dot beads, which were sold by mass merchandisers nationwide from April 2007 through November 2007, please check store and local news sites for Washington product recall information. If you believe that your child has ingested Aqua Dot beads, contact your physician immediately. And call the Seattle personal injury attorneys at Bernard Law Group, 1-800-418-8282, or visit our website, www.4injured.com

October 31, 2007

Baby Cold Medicines Potentially Harmful

Drug companies have voluntarily withdrawn over-the-counter cough and cold medicines for children under 2 years old, after federal regulators and private doctors warned of potential health risks to infants and toddlers.

The withdrawn products include the following over-the-counter infant cold medicines: Tylenol, Dimetapp, Robitussin, Triaminic, and Little Colds.

Continue reading "Baby Cold Medicines Potentially Harmful" »

October 22, 2007

Medtronic Sprint Fidelis Recalls Faulty Defibrillator Leads

Sprint Fidelis defibrillation leads made by Medtronic Inc have been removed from the market, due to five patient deaths linked to these devices, as well as other serious complications caused to patients.

A defibrillator is used to regulate a person’s heartbeat. When it senses an abnormal heart rhythm, it then delivers an electronic shock to reset the heart to a normal beat. If there is a fracture in the lead, it can cause the defibrillator to send unnecessary shocks to the heart, or fail to work at all.

Continue reading "Medtronic Sprint Fidelis Recalls Faulty Defibrillator Leads" »