Toxic Chinese Drywall Problem More Extensive than Initially Reported

In the first decade of this century, the construction industry across Tennessee, North Carolina and the rest of the U.S. boomed. It was also during this time that millions of tons of sheetrock were imported from China.

According to the Chinese Drywall Complaint Center, it’s estimated over 500 million pounds of drywall (…or sheetrock) containing a variety of toxins were imported. Ordinarily, drywall for domestic construction is manufactured entirely in the U.S.  In response to increased demand though, the import of Chinese drywall began around 2001 and accelerated rapidly following the disastrous hurricanes in 2004 and 2005 (…especially Hurricane Katrina).

By all available evidence, import of Chinese drywall ended in 2007 when the housing boom started to cool.

The damage was done though, especially in homes in the Deep South. Figures show Florida was the hardest hit state but the toxic drywall is considered to be a national problem. Any area with high heat and humidity – which we see plenty of here – can cause the toxic drywall to become a real nuisance, even real danger.

It’s also been reported that homes in Canada may have toxic drywall imported from China as well.

Toxic drywall can be quite noticeable if conditions are right. Laboratory samples have identified emissions of carbon disulfide, carbonyl sulfide and hydrogen sulfide – each are substances that pose tremendous hazards to human health.

These emissions smell like rotten eggs, which is certainly noticeable, and unpleasant.

Homeowners with toxic drywall have reported a variety of health problems, including asthma attacks, chronic coughing, difficulty breathing, chronic headaches and sinus issues.

Corroded A/C Coils

In the home itself, the toxic drywall causes all sorts of issues, many of which are found in copper wiring and components found in electrical wiring, A/C systems and even electronic devices like TVs and radios. Reactions with hydrogen sulfide cause copper components to turn black and powdery.

It’s even been reported that silver jewelry can be ruined by this reaction.

Absent of these reactions, the only way to find out if you have toxic drywall is to tear sections off and look on the other side of the drywall. It’s estimated that toxic drywall from 20 companies was imported into the U.S. between 2001 and 2008. Many of these companies, like Knauff-Tianjin, are currently facing several lawsuits.

If you discover your home has toxic Chinese drywall, it can cost thousands to repair. While some homeowners in Florida and elsewhere have received compensation, the process in quite chaotic, especially considering the lack of federal involvement in the issue.

If you’re looking to purchase a home built between 2001 and 2008, be sure you get a thorough inspection to insure the home doesn’t have toxic Chinese drywall. This is especially important if the home is a foreclosure.

And if you’re experiencing problems in your home and believe it’s due to toxic drywall, click on over to the Chinese Drywall Complaint Center for more information. There you can find sample letters to provide your lender and more about what to look for in your home.

While Tennessee and North Carolina hasn’t experienced the brunt of this problem, there are still many homes in our region that have this toxic substance. If you’ve been adversely affected, contact Tennessee product liability attorneys at Gilreath & Associates to discuss your options today.

Defective Airbags Prove Dangerous for Many Passengers

When airbags were introduced, car makers and safety advocates hailed it as a seminal moment in vehicle safety, comparing them to the advent of seatbelts in the 1970s.

While airbags have helped reduce the physical impacts of car collisions, they do carry some danger.

Anyone with a newborn is certainly, or at least should be, aware that their child should be seated in the back of the vehicle. If they must sit in the front (…like in a single-cab pickup), the airbag should be disabled. Elderly folks too have to be careful around airbags since the impact of one could prove devastating.

Even though airbags have helped make cars safer, they’ve also proved to be very dangerous in the event they malfunction.

“We’ve seen a lot of cases where the person has a fender bender, the airbag goes off and hits them in the face, and they’ve lost an eye,” explains Raymond Bodiford, senior partner at the Bodiford Law Group in Orlando, Florida.

Below are some of the common malfunctions that can occur with an airbag:

  • Failure to deploy
  • Accidental deployment
  • Late deployment

While many may be familiar with the first two types of malfunctions, the third can pose serious risks as well. Late deployment basically means the airbag deploys after the accident has occurred.

“It can actually cause additional damage because the force of the accident has usually positioned the occupant too close to the airbag at the time it deploys,” explains Bodiford.

One example of defective airbags can be found in Honda vehicles built between 2001 and 2003. Starting in 2008, thousands of Honda vehicles were recalled because of a defective airbag inflator on the driver’s side. This defect was said to have caused 12 injuries and at least one death.

Since the initial recall, Honda has expanded it to include various Accord, Civic, Odyssey, CR-V, Pilot and Acura models. The most recent recall was issued by the company on December 2, 2011.

Most injuries from airbags occur in the chest area since it deploys at over 100 mph. Deploying airbags though can also cause burns. More serious injuries can occur in the neck area if the driver/passenger is of a certain height.

Although rare, deploying airbags can cause fatality. From 1990-2000, over 175 fatalities from airbags were reported by the National Highway Traffic and Safety Administration. The agency though estimates that of the approximately 3.3 million airbag deployments, more than 6,377 lives have been saved and countless injuries prevented.

Tennessee Court of Appeals Weaves Winding Preemption Path in Seat Belt Failure Cases

The Tennessee Court of Appeals, Western Section, has commented on the application of recent U. S. Supreme Court cases involving product failure cases, specifically cases involving injury and death resulting from how auto manufacturers design seat belt systems in their cars and minivans.  In the case of Clifton Lake et al v. The Memphis Landsmen, LLC et al, Case No. W2011-00660-COA-RM-CV, the Tennessee Court of Appeals decided to follow the framework set forth by the U. S. Supreme Court in Geier v. American Honda Motor Co., 529 U.S. 861, 120 S.Ct. 1913, 141 L.Ed.2d 914 (2000), which held that when the Federal Motor Vehicle Safety Administration issued regulations giving auto manufacturers a choice of whether to install lap belts or shoulder harness seatbelts in vehicles, regulation of seat belt systems was a significant objective of the regulations, meaning that state court lawsuits challenging a manufacturer’s design of those systems were pre-empted by federal regulation, and individuals were bringing suit to challenge the design were preempted.  The effect of the Geier decision was to make it more difficult for injured citizens to bring suit challenging the design of a car or minivan’s seat belt restraint system when occupants were injured or killed as a result.

In this most recent decision, the Tennessee Court of Appeals dealt with application of  Geier in relation to another more recent U. S. Supreme Court decision, Williamson v. Mazda Motor of America, Inc. et al, 131 S.Ct. 1131, 179 L.Ed.2d 75 (2011).  In Williamson, the U. S. Supreme Court dealt with the issue of whether permimtting a state court suit attacking the manufacturer’s choice of using only a lap belt to continue would constitute a denial of a manufacturer’s ability to choose which seat belt system to use in its automobile design, or whether the issuance of federal motor vehicle safety regulations giving manufacturers the choice preempted state court lawsuits challenging the design of seat belt systems in its vehicles.  On its face, the issue in Williamson appeared to be the same as in Geier, and therefore the Lake case as well.

The U. S. Supreme Court in Williamson tangled with the issue of preemption.  In particular, the Court noted that the regulations at issue contained one clause expressly preempting certain lawsuits, another clause expressly allowing certain lawsuits to be brought (called a “savings clause”), and then addressed the issue of whether or not the state court lawsuit in question constituted a suit in conflict with the safety regulation, noting that longstanding federal decisions held that when a state court lawsuit conflicts with the objective of federal regulations, the regulations preempt the state court lawsuit, meaning the state court lawsuits could not be brought and must be dismissed.    After stating the general principle of Geier that state court lawsuits attacking seat belt design restricted the choice given to manufacturers in federal safety regulations, and were therefore preepmpted, the Court in Williamson found circumstances that led it to conclude that the legal issue in play in Williamson did not represent an issue dealing with a significant objective of the federal safety regulation, and therefore, even though the state court lawsuit conflicted with federal safety regulations, the state court suit at issue in Williamson was not preempted.

Why the difference?  Between the time of the Geier case and the Williamson case, the Federal Motor Carrier Safety Administration changed its rules concerning manufacturer choice of set belts in passenger vehicles, specifically minivans.  The U. S. Supreme Court in Williamson specifically analyzed not only the language of the two regulations, but looked into the intent and purpose for the change.  The Court found that the original regulation in Geier represented a balance between safety but also consumer acceptance.  At the time of issuance, mandating shoulder harness belts was not yet the norm in the U.S.  By the time of Williamson, shoulder harness belts were commonplace, and the new regulations were speficially drafted to address safety concerns alone, not consumer acceptance.  The Court found that the DOT was much less concerned with practical issues of whether shoulder belt harnesses were cumbersome or restrictive, and was instead focused squarely on pure concerns of increased safety.  Indeed, the Court noted that the DOT itself did not believe that state court suits conflicted with seat belt regulations, since it considered the federal regulations to be minimum standards, meaning that state court lawsuits on seat belt design did not conflict with DOT regulations, since any effort to increase safety in use of seatbelts only enhanced the purpose of the regulations.  In short, the regulation at issue in Williamson did not consider manufacturer choice to be of concern – only safety, and since the state court lawsuit was also concerned with safety, it did not conflict with federal safety regulations and was therefore permitted to exist.

Taking all of this in perspective, Tennessee Courts have again demonstrated their willingness to chart their own path, regardless of what the U. S. Supreme Court says.  Writing for the unanimous majority, Judge Steve Stafford opined that the Williamson case provided no justification to conclude that plaintiffs’ case in Lake should be permitted, since under Geier, the Court reasoned it should be preempted.  The Lake case involved a man who was injured when the commercial shuttle bus he was riding in was involved in a collision in Memphis.  The bus in question had large tempered glass windows, “perimeter seating” where all seats faced toward the middle of the vehicle, and no seat belts.  This type of vehicle is commonly used for transportation between airports and rental car facilities, and some courtesy shuttles.  The plaintiff in Lake was ejected from the vehicle during the collision, resulting in a serious brain injury.  The lawsuit filed against various defendants charged that the shuttle was defective in design because it did not contain seatbelts, that perimeter seating was inferor, and that the use of tempered glass was inappropriate.  At trial, a jury found in favor of the plaintiff, awarding more than $8 million in damages, but placed all fault for the collision on the driver of a concrete truck, who had caused the collision to occur.  Plaintiffs filed a motion for new trial, and the Tennessee Court of Appeals, Western Section, ruled that a new trial was not warranted on the defective product theories about seat layout, use of tempered glass, and lack of seatbelts, because cases like Geier held that state law personal injury cases involving seat belt claims were preempted.  In the meantime, the U. S. Supreme Court decided Williamson, and the plaintiffs appealed to the Tennessee Supreme Court, asking the Tennessee Supreme Court to review the case in light of Williamson.  Instead, the Tennessee Supreme Court instructed the Western Section Court of Appeals to address the case in light of Williamson. After analyzing Williamson and Geier, the Western Section concluded that Williamson was a very narrow decision, concluding that Geier represented the general rule of law.  In particular, the Western Section determined that the lesson of Geier and Williamson was that in seat belt cases, the fact that regulations gave manufacturers a choice of which seat belt system to use was not determinative of whether or not a state law case could be maintained.  Instead, the Western Section found that the issue of manufacturer choice must be made in furtherance of a “specific regulatory objective” in order for state law tort claim to be preempted.  In this way, the Western Section appeared to adopt the framework of Williamson.  The Western Section also took from Williamson that the proper analysis requires that the Court look to the purpose and intent of the regulations to determine what the significant objectives of the regulations were, for purposes of determining whether a state court suit was preempted.   On the tempered glass claim, the Western Section found that plaintiffs’ claims did conflict with federal regulations, since built into the regulations on glass was a choice given to manufacturers.  The Western Section snapped back into a Geier analysis, reasoning that Williamson never supplanted Geier, it just distinguished it based on the facts of the Williamson case alone.  Similarly, the Western Section employed the same approach on plaintiffs’ seat belt and seating claims.  Overall, the Western Section took the perspective that it’s pre-Williamson ruling was sound, and need not be altered, since Williamson was a narrow, fact-driven decision that did not change the inherent rule of law espoused in Geier.

Based on the Lake decision from the Western Section Court of Appeals, Tennessee law follows Geier when facing state law claims involving seat belt and restraint system failures.  Presumably, Tennessee jurisprudence would apply equally to any state law personal injury claim asserting a defect in motor vehicle safety.  It remains to be seen if the Tennessee Supreme Court will take up Lake and further reflect on this analysis.

Keep Your Kids Safe this Christmas Season – Toy Safety

With the Christmas season in full swing, we’re all looking forward to the holidays with anticipation. In all of this excitement though, it’s easy to forget about toy safety and keeping our kids injury free.

Many of us here in the firm are parents – even grandparents in fact – and take toy safety quite seriously, especially during the holiday season. Over 3 billion toys are sold annually in the U.S. – 60% of those sales occur during this time of year.

Over the year, we see many toy recalls issued for a wide range of hazards, including:

  • Choking
  • Strangulation
  • Falls
  • Laceration
  • Burns

And in our firm, we do see the occasional case of a child being injured by a defective or dangerous toy.

Taking a few easy steps though can prevent your holiday from becoming a trip to the emergency room.

First, only buy toys suitable for the child’s age, abilities and skills. For example, it wouldn’t be a good idea to buy Legos for a toddler since they can pose a choking hazard. Toys with small parts in fact shouldn’t be given to children under 3.

Follow the manufacturer’s instructions for proper assembly and use as well. Even if something happens and you have to pursue a defective product claim, the manufacturer will likely first claim you weren’t following the instructions and therefore, deny liability.

And for certain toys like bicycles, roller skates and scooters, you need to have additional safety equipment for your kid. Helmets, knee pads and other items to prevent scrapes and head injuries are important. Bicycle helmets in fact are required for anyone under age 16 in Tennessee.

Other toy hazards to be on the lookout for include:

  • Sharp edges and points
  • Tiny parts
  • Loud noises
  • Projectiles, or anything that can be propelled
  • Electric toys that can burn or shock

Taking a few precautionary steps can ensure your children stay safe this holiday season. Christmas is supposed to be a special time of year. Don’t let your child be one of the approximately 150,000 accidents from toys that occur each year according to the U.S. Consumer Product Safety Commission.

In closing, all of us at Gilreath Law wish you and yours a very Merry Christmas and Happy New Year.

We look forward to bringing personal injury, medical malpractice and other Tennessee legal news/updates to you in 2012.

Shoulder Pain Pump Injections Pose Devastating Risks

Injury to the shoulder(s) often result from falls, especially if they were off a ladder or higher up off the ground. To repair the damage, arthroscopic (shoulder) surgery is often used. Following this procedure, the patient will still be in a lot of pain.

While oral medications are used much of the time, direct injection of pain medication through a catheter is sometimes used.

This direct injection method helps provide needed relief from pretty serious pain. However, many patients who have received pain medication through this method claim the injections led to a much more serious condition known as Postarthroscopic Glenohumeral Chondrolyosis, or PAGCL.

PAGCL is characterized by a progressive loss of cartilage in the glenohumeral joint, which connects the arm and shoulder together.

This cartilage cannot regenerate and therefore its loss is permanent, which causes severe pain, discomfort and a life-long disability. Other indications of PAGCL include:

  • Increased shoulder pain both when resting and moving
  • More stiffness in the shoulder
  • Clicking, popping and grinding in the shoulder
  • Loss of strength and decreased range of motion
  • X-ray will show narrowing joint space

Complaints from patients led the American Academy of Orthopedic Surgeons to commission a study in 2006 where 152 shoulder surgery patients were examined. Of these patients, 12 developed PAGCL, all of which received pain pump injections directly into the shoulder.

Patients who only received injection(s) to the soft tissue surrounding the shoulder did not experience breakdown in cartilage…this much shorter injection is in fact the only method approved by the U.S. Food & Drug Administration.

In an advisory released a few months ago, the FDA asked manufacturers to include warnings about direct injection. However, the agency doesn’t openly say pain injections cause cartilage breakdown, maintaining they do not know why this occurs in some patients.

Regardless, many lawsuits have been filed by patients seeking compensation for damages resulting from the use of pain pump injections.

If you’re experiencing symptoms listed above and have had direct injections of pain medication to your shoulder, it’s important you consult with your doctor immediately.

It’s also suggested you contact a medical malpractice or defective product attorney licensed in your state. Tennessee medical malpractice attorneys at Gilreath & Associates can help you obtain compensation for injuries stemming from defective products like this.

Steering Problems Prompt Recall of 420,000 Toyota and Lexus Vehicles

In the last 2-3 years, Toyota drivers have been bombarded with several recall warnings. Stuck accelerator pedals proved to be the most deadly (…and numerous in terms of the number of recalled vehicles).

This time, steering problems are leading the Japanese automaker to recall 420,000 of some of its most popular models, including:

  • 2004 Toyota Avalon
  • 2004-2005 Toyota Camry, Highlander, Sienna and Solara
  • 2006 Highlander HV
  • 2005 Lexus ES330 and RX330
  • 2006 Lexus RX400h

Each of these models comes with either a 1MZ-FE or 3MZ-FE V6 engine.

The issue at hand involves an inadequate amount of adhesive between the outer and inner ring of the crankshaft pulley. This lack of adhesive could potentially cause the outer ring to become misaligned and lead to a malfunction in the vehicle’s steering.

If the outer ring becomes misaligned, drivers will hear a strange noise coming from the engine compartment according to the automaker’s advisory on the matter. This defective ring could also cause the alternator to slip on the pulley and cause a decrease in power. Eventually, all battery power can be depleted if the situation isn’t addressed.

Toyota is currently working to obtain the needed parts. Affected owners will be notified sometime in January to bring their vehicles to a dealer for inspection and repair.

If you have any questions or think you have a problem related to this issue, contact Toyota at (800) 331-4331 or Lexus at (800) 255-3987.

And if you or a loved one has sustained injury due to this or any other malfunctioning product, contact Nashville defective product attorneys at Gilreath & Associates today for a free consultation.

Research Shows E-Prescriptions as Prone to Error as Handwritten Ones

Submitting prescriptions electronically has been lauded by the healthcare industry and policy makers alike as a way to reduce errors and costs. However, research recently published in the Journal of American Medical Information Association concludes that prescriptions sent electronically are just as likely to contain errors as ones written out by hand.

A clinical panel reviewed 3,850 computer generated prescriptions that were received by a commercial pharmacy chain in 3 states in 2008. The panel reviewed the prescriptions for medical errors and examined whether any of the mistakes could pose harm to the patient.

If the nearly 4,000 prescriptions analyzed, 11.7% of them contained some sort of error. Of all of the prescriptions, 4% had errors that could pose some sort of harm to the patient (…most were considered ‘serious’ or ‘significant’ events but none were life-threatening).

According to authors of the study, this is about the same rate of error found in handwritten prescriptions. Researchers though concede to one limitation of their findings – they were unable to determine whether a prescription was sent electronically to the pharmacist or was prepared on a computer, printed out and given to the patient.

“Although most evidence suggests enthusiasm for a more paperless system is well founded, new technology can also introduce new potential for medication errors,” comments Karen Nanji, MD, of Massachusetts General Hospital in Boston and one of the study’s authors.

Errors in the electronic prescriptions were highest among anti-infectives, accounting for 17.3% of the mistakes. Nervous system drugs and respiratory drugs constituted the 2nd and 3rd most common errors respectively.

Of the errors, nearly 2/3 of them consisted of omissions of important information like duration, dose or frequency. Other errors simply consisted of confusing information – like telling a patient to take the drug ‘as directed’ but not expanding any further.

One error for example included instructions for the patient to take five, 500 mg Vicadin tablets every four to six hours.

“Implementing a computerized prescribing system without comprehensive functionality and processes in place to ensure meaningful use of the system does not decrease medication errors,” the study concluded.

Authors of the study also outlined ways healthcare providers could reduce errors, like programming systems so they do not allow omission of information, incomplete drug names or inappropriate abbreviations.

Having errors on your prescription could lead to disastrous consequences, even death in some cases. If you’ve been adversely affected by an error on your prescriptions, you may be able to pursue a medical malpractice claim in Tennessee.

If you or a loved one has experienced a situation like this, it would behoove you to speak with a medical malpractice attorney in Tennessee experienced in helping patients adversely affected by prescription errors.

Under Tennessee laws, you only have 1-year from the date the prescription was issued to pursue a case and obtain compensation for medical costs, lost wages from work and damages for pain and suffering.

Off-Road Buggies Recalled Over Broken Steering Controls

Approximately 3,200 Bad Boy Buggy off-road vehicles have been recalled after more than a dozen reports of broken steering controls.

The recall was issued last week by the U.S. Consumer Product Safety Commission after BB Buggies, Inc. and Bad Boy Enterprises, LLC received 15 reports of broken steering assembly arms. Fortunately, no injuries have been reported in connection with this defect.

Defective or broken steering assemblies can pose a crash hazard. Riding in these hills here in Tennessee, this kind of defect could lead to some terrible accidents.

Several models of these electric off-road vehicles are affected by this recall, including Bad Boy’s LT, Classic, XT, XTO and XT Safari models. Affected models come in a camouflage, hunter green or black color and have ‘Bad Boy’ printed on the side and front. They were sold between August 2009 and June of this year for between $7000 and $15,000.

The CPSC recommends you discontinue use immediately and contact an authorized dealer or BB Buggies for free replacement parts. Any questions about replacement items should be directed to the company by calling (855) 738-3711 or visiting their website at http://www.badboybuggies.com/.

This is the 3rd recall for Bad Boy Enterprises, LLC in as many years.

In October 2009, nearly 4,000 of the company’s Classic Buggies were recalled due to acceleration problems. After determining this recall failed to address the problem, another 9,300 buggies were recalled in December of last year. Each these recalls came about because consumers called the company about their concerns.

If you have a problem with something you own, it’s important you notify the company of the potential hazard. Hazards that arise due to defects are the responsibility of the manufacturer and need to be addressed accordingly.

But if something happens all of a sudden due to a defective product, you do have the right to pursue legal recourse. Our Tennessee firm handles many of these types of product liability cases. Contact us today to discuss your individual case.

Child Safety Latches and Outlet Covers Subject of Recall

The U.S. Consumer Product Safety Commission (http://www.cpsc.gov) announced today that Prime-Line Products, an importer located in Redlands, California, had agreed to a voluntary recall of 37,000 child safety latches and outlet covers, based on the discovery that screws on the safety latches can loosen and/or break, allowing young children to gain access to unprotected electrical outlets and small loose parts they could ingest.  The products were sold under the name Child Safe.  The recall includes child safety drawer and cabinet latches, as well as outlet covers with rotating receptacle covers.

Identification of unit numbers can be found here: http://www.prnewswire.com/news-releases/child-safety-latches-and-outlet-covers-recalled-by-prime-line-screw-breaks-can-allow-unintended-access-126251038.html

Prime-Line was the importer of the products, all of which were made in China.  The products were sold at various big box hardware retailers, including Ace Hardware, Friedman Brothers, Menards, Orgill, True Value, Do-It-Best, and others.

Photos of the subject products can be seen here: http://www.cpsc.gov/cpscpub/prerel/prhtml11/11284.html

Gilreath & Associates is experienced in handling serious injury cases caused by product failures and defects.  If you believe a lived one has been injured or killed as a result of a product failure or defect, please contact us to discuss your situation in detail at 1-800-637-7024.

185,000 Pounds of Ground Turkey Recalled Due to Salmonella

As the nation remembered the harrowing events of Sept. 11, 2001, a recall for 185,000 pounds of ground turkey produced by Cargill was issued by the U.S. Food Safety & Inspection Service.

Issuing the Class I recall on Sunday, the food inspection agency claims the turkey contains Salmonella Heidelberg, the same strain that prompted a similar recall in August. The recall affects fresh ground turkey sold nationwide, including Kroger stores here in Tennessee.

All of the products under this recall were produced at Cargill’s plant in Springdale, Arkansas. The original recall issued on August 3rd for an astounding 36 million pounds of ground turkey halted production at the plant for two weeks. State and federal health inspectors tracked the source of a salmonella outbreak to meat produced at the plant.

But after only a few weeks back online, the plant is once again under fire.

The latest recall is for ground turkey produced at the plant on August 23-24 and August 30-31. Considering the same type of salmonella bacteria is still in the meat, the source of the contamination is either at the Springdale plant or somewhere in the chain of production.

While there haven’t been any illnesses associated with this latest recall, at least 107 illnesses and one death were reported in connection with the original recall.  As of this writing, two lawsuits – one by a man in Arizona and another from a toddler’s parents in Oregon – have been filed against Cargill.

Affected products will have an establishment number of P-963 inside the packaging’s USDA mark of inspection. Specific products will have use or freeze by dates ranging from 9/11/2011 through 9/21/2011. Products specifically sold at Kroger stores include:

  • 48.0 oz. (3 lb.) trays of Kroger Ground Turkey Fresh 85/15 with Use or Freeze by Dates of 09/17/2011, 09/18/2011 and 09/19/2011
  • 16 oz. (1 lb.) trays of Kroger Ground Seasoned Turkey Patties Fresh 85/15 with a Use or Freeze by Date of 09/17/2011

A Class I product recall is the highest level issued by the FSIS and means there’s a reasonable chance of illness and maybe even death, especially in young children and the elderly.

Any questions regarding this recall should be directed toward Cargill consumer relations hotline at (888) 812-1646.

Prevention is your best protection against salmonella and other food-borne illnesses. Wash your hands with warm, soapy water for at least 20 seconds before and after handling raw meat. And cook ground turkey and beef to an internal temperature of 165 degrees Fahrenheit.

If you’ve purchased one of the products affected by this recall, return it to the store for a full refund. And if you or a loved one fallen ill due to contaminated products like this, you may be entitled to legal compensation. Contact defective product attorneys at Gilreath Law in Nashville, Knoxville and Memphis today for a free consultation.