Drop-Side Cribs Outlawed After Multiple Deaths

After millions of recalls and more than 30 infant and toddler deaths, the government outlawed drop-side cribs yesterday.
The Consumer Product Safety Commission voted unanimously to ban the manufacture, sale and resale of the cribs, which have a side rail that moves up and down, allowing parents to more easily lift their child from the crib.
The new standard requiring cribs to have fixed sides would take effect in June. The move by CPSC would also prohibit hotels and childcare centers from using drop-sides, though those facilities would have a year to purchase new cribs.
CPSC Chairman Inez Tenenbaum said, "I believe these new standards will markedly reduce crib-related hazards and help to ensure that young children sleep more safely in their cribs."
Around for decades, drop-side cribs have come under scrutiny in recent years because of malfunctioning hardware, sometimes cheaper plastics, or assembly problems that can lead to the drop-side rail partially detaching from the crib. When that happens, it can create a dangerous "V"-like gap between the mattress and side rail where a baby can get caught and suffocate or strangle.

Toyota Recalls 2011 Sienna

Toyota’s list of recalls continues to grow. The automaker is voluntarily recalling 94,000 2011 Toyota Sienna minivans. The affected vehicles were produced before early November 2010.

“The recall is a result of a Stop Lamp Switch Bracket placed near the parking brake,” Autoblog explains. “When the parking brake is fully applied it may deform the switch bracket. This could result in the brake lights remaining lit or even partial engagement of the brakes resulting in a reduction of brake effectiveness over time.”

While this recall adds to the millions of vehicles Toyota red flagged in the past year, there is some good news. No accidents, injuries or deaths had resulted from the faulty bracket.

Toyota explains that Sienna owners “will receive an interim notification advising them of this recall by first class mail beginning in mid-January 2011, along with instructions for what to do if they experience this condition and how to minimize the possibility of inadvertently contacting the stop lamp switch bracket while operating the parking brake. Toyota will also post this information on its website.”


Owners will get another notification in February in mid-January 2011. At that time, they can make an appointment at any Toyota dealer to remedy the problem free of charge.

Joseph Messa Nominated to ABF

Joseph Messa has been nominated to become a Fellow of the American Bar Foundation (ABF). It is an honor to be chosen, as less than one third of one percent of US lawyers are members. ABF members support ground breaking research in law and social science and participate in educational programs at the American Bar Association's (ABA) Midyear and Annual Meetings.
Founded in 1952 by the ABA, the ABF is recognized as the premier institute for social science research on law in America. Among its research faculty is 2000 Nobel Prize winner in Economic Sciences, James Heckman. Other notables include John Hagan (awarded the 2009 Stockholm Prize in Criminology) and Steven Levitt (author of the bestseller Superfreakonomics).

Johnson & Johnson Issue Recall . . . Again

There's more trouble for Johnson & Johnson. The company issued a recall of nine million liquid Tylenol cold medicine bottles. The product was mislabeled and did not warn consumers the medicine contained alcohol. Three separate Tylenol Cold Multi-Symptom liquid products were recalled. The FDA requires manufacturers to list alcohol as an ingredient when used. However, these bottles did not acknowledge that alcohol was used in the flavoring agents.

A few days earlier, McNeil (a Johnson & Johnson division) recalled 800,000 bottles of junior strength Motrin and four million packages of children's Benadryl. Both products failed to meet manufacturing standards but the company says no threat was posed to consumers.

The Tylenol recall affects Tylenol Cold Multi-Symptom Daytime 8 oz Citrus Burst Liquid, with an NDC Code of 50580-257-08’ Tylenol Cold Multi-Symptom Severe 8 oz Cool Burst Liquid, with an NDC Code of 50580-351-08; and Tylenol Cold Multi-Symptom Nighttime 8 oz Cool Burst Liquid, with an NDC Code of 50580-269-08.

Fabric Protector Recalled Due to Respiratory Hazard

Claire-Sprayway Inc. and the U.S. Consumer Product Safety Commission issued a voluntary recall of Fabric Protector.  Overexposure to fumes, vapor or spray mist from the product can pose a serious respiratory hazard to consumers.
The firm has received 36 incidents of overexposure to fumes, vapor or spray mist, 34 of which involved coughing, wheezing or shortness of breath. One incident resulted in a serious respiratory injury.

The fabric protector was sold under the following brand names: Sprayway® No. 980 Industrial Fabric Protector; 3D Fabric Protector; Auto Brite Fabric Protector Guardatela; Auto Magic® Fabric Protector No. 91-S; Crystal Aire Products #680 Fabric Protector; Falcon Labs® Spotless Fabric Protector; Quiltprotect™ Spray; Robbie’s™ Fabric Shield; Showcar Fabric Protector and Simoniz® System 5 Stain Sentry Fabric Protector. The can size is 13.5 oz., and the product code is located on the bottom of the can.

The product was sold at automotive supply, auto detailing, upholstery, textiles, furniture and fabric stores nationwide from January 2005 through August 2010 for about $10.

Munchkin Recalls Bathtub Toys Due to Injury Risk

Munchkin and the U.S. Consumer Product Safety Commission issued a voluntary recall of Bathtub Subs do to a laceration hazard.  The toy submarine's bottom can suck up loose skin and injure children.  CPSC and the company are aware of 19 incidents of lacerations to boys' genital area. One of the incidents required medical attention.

This recall involves battery-operated bathtub submarine toys. The toy is yellow, has a smiling face, turquoise windows, an orange propeller and an orange periscope that turns the toy on and off. The intake valve has a water pump that sucks in water to propel the submarine. The toy is intended for use by children during bath time.

The submarine was sold at retail and children's stores nationwide from November 2009 through September 2010 for about $7.

Help Local Families this Thanksgiving with Tons of Turkeys

As part of the Messa & Associate's mission to help the local community, the firm made a donation to Tons of Turkeys.  The local, family-run nonprofit helps provide turkeys to 100s of underprivileged families throughout Philadelphia and the surrounding suburbs.  To learn more about the organization and make a contribution, visit www.tonsofturkeys.org.

Defective Drugs--Digitek

Even after a drug is known to be defective, it can pose a threat to consumers.  This is the case with Digitek.  A lawsuit has been filed against manufacturers Totowa and Mylan Pharmaceuticals, stating the companies knew the drug was defective yet still released it in "safer" single doses.  Allegedly, the plaintiff's son received a double dose and died.  The prosecution believes the manufacturers had the responsibility to design, manufacture and sell safe drugs to the public. 

Meridia--Higher Chance of Problems than Benefits

The prescription weight loss drug Meridia was withdrawn from the US market last month. The drug, manufactured by Abbott Laboratories, is linked to heart problems including heart attacks and strokes. While these were among the reported side effects, the FDA could no longer justify the drug after comparing Meridia's weight loss benefits to the risks.


A study found when taking the drug a person's chance of stroke, heart attack and death increases by 16% compared to those taking a placebo. In comparison, there was only a 2.5% body weight difference. Since, the FDA encouraged Abbott Laboratories to voluntarily recall Meridia.

Electrolux and Frigidaire ICON Recall

Due to a fire Hazard, Frigidaire and Electrolux ICON have issued a voluntary recall of the Smoothtop Electric Cooktops and Frigidaire Slide-in Ranges with digital displays and rotary knobs.  The products were manufactured by Electrolux Home Products Inc. 

Electrolux has received reports of liquids gathering under the control knob and causing the surface heating element to turn on unexpectedly, heat to high temperatures and then turn off.  This malfunction poses a burn hazard to users and fire hazard. 

The serial and model numbers for the cooktop models can be found on the underside of the surface.  For the slide-in ranges, numbers can be found inside the oven door on the left.  The recalled products' model and serial numbers are:

Honda Recall

Honda Motor Co. announced they are recalling vehicles due to brake fluid leaks, which can lead to weaker braking power.  Some brake fluid types negatively affect the brake's master cylinder seal. About 500,000 vehicles are being recalled.  The affected cars are 2005-2007 Acura RL sedans and 2005-2007 Odyssey minivans.

More Toyota Recalls

Toyota made a recall announcement today involving 1.53 million Avalon, Lexus and other car models across the U.S. and Japan. The recall is a result of problems with the cars' fuel pumps and brake fluids. In the U.S., about 740,000 cars will need to be taken back for repairs. The company has already recalled over 10 million cars in the past year.
Most cars have glitches in the brake master cylinder. The problem could mean weaker braking power. The specific models are the 2006 Lexus GS300, IS250, and IS350, 2004 through 2006 Lexus RX330 and non-hybrid Highlander and the 2005 through 2006 Avalon.

Jogging Strollers Pose Strangulation Hazard, Recalled

Tike Tech has issued a voluntary recall of their Single City X3 and X3 Sport Jogging Strollers due to a strangulation hazard.  The opening between the seat bottom and grab bar could potentially allow an infant's body to pass through and become trapped at the neck by the grab bar, if the child is not harnessed.  In general, parents are encouraged to secure children in strollers using safety harnesses.  Children should never be left unattended in their stroller. 

The recalled strollers' ID codes end in 01, 02, 03, 04, 05, 06 and 07.  All codes begin with TT-18 and can be found on the left side of the frame interior.  The strollers were sold for about $300 between October 2009 and February 2010. 

Ryobi Recalls 455,000 Cordless Drills

Ryobi Technologies Inc. announced they're recalling 455,000 cordless power drills. The company has received reports of the tools overheating and causing property damage and minor burns. The recalled drill is the Ryobi Model HP 1802M. There have been 47 reports of the tool catching fire, melting, smoking or overheating.


The drills feature the brand name on the left side in white and red, are black and blue and were sold exclusively at Home Depot Inc. from January 2001 to July 2003 for around $100. If you own this drill, immediately stop using it and report any incidents to the U.S. Consumer Product Safety Commission.

Mercedes-Benz Recall

Luzury car maker, Mercedes-Benz SA, is in the process of fixing over 85,000 cars worldwide with faulty steering mechanisms.  Today, they announced the recall of 3,085 cars, including C-Class and E-Class models.

Affected customers will be notified and repairs will be free of charge at authorized Mercedes-Benz dealers.  The power steering system of those C and E-Class cars produced between June 2009 and February 2010 can potentially leak power steering fluid.  Such a leak can cause higher than normal required steering forces. 

Alexander Designs Recalls Cribs Due to Fall, Entrapment and Suffocation Hazards

Alexander Designs recalled its drop-side cribs, which were sold exclusively at JCPenney.  The crib's drop-side rail can break causing it to detach.  If it detaches, a dangerous gap is created.  The drop-side can malfuntion due to incorrect assembly or because of age related wear and tear. 

The recalled cribs were sold under the Alexander Designs Ltd. brand and have the item number printed on the crib's headboard label.  The cribs being recalled are:

September Car Recalls

BMW, Rolls-Royce

Around 345,000 BMW 5, 6 and 7 Series with V8 and V12 engines and 6,000 Rolls Royce Phantom cars have been recalled worldwide.  According to a BMW spokesperson, another 150,000 BMWs could be added to the recall.

To date, there have been no reported injuries caused by the vehicles.  They are being recalled due to potential brake problems—some brake systems are more difficult to use after a long period of operation. 

Hyundai Sonata 2011

Due to steering column problems, Hyundai is recalling 140,000 2011 Sonata sedans.  The column can malfunction causing the driver to lose steering ability.  The cars at risk are Hyundai Sonatas produced between December 11, 2009 and September 10, 2010.  While there have not been any reported accidents, Hyundai has received complaints from drivers reporting abnormal sounds and feeling looseness. 

Bentley

Bentley issued a recall of Brooklands, Azure and Arnage models due to the possibility the “Flying B” hood ornament could impale pedestrians.  The recalled cars were sold between October 2006 and October 2009 for around $246,999 and $363,000.  By design, the Flying B retracts if there’s a collision.  A few instances showed the B did not retract as quickly as it was supposed to.  No reports of injuries to pedestrians have been filed to date.

Cadillac CTS

In collisions, certain Cadillac CTS models could potentially cause leg injuries.  General Motors has issued a recall of the 2009 and 2010 Cadillac CTS all-wheel-drive cars and CTS-V performance sedans.  The recalled Cadillacs do not comply with federal safety requirements.  Smaller passengers in the front seat could sustain injury to the femur if not wearing a seatbelt. 

Cordless Electric Lawnmowers Recalled Due to Laceration Hazard

Black & Decker and Craftsman announced a voluntary recall of their cordless electric lawnmowers.  Although removing the safety key is intended to stop the motor and blade, there have been over 30 reports of the motor operating even after the safety key is removed.  Two of those reports involved finger lacerations. 

About 16,000 cordless electric lawnmowers were sold across the country at hardware, discount and home center stores between September 1995 and December 2006 for $450.  The Craftsman brand version was sold at Orchard Supply Hardware and Sears between Junly 1998 and December 2000 for $450.

The Black & Decker mowers' model numbers are CMM1000 and CMM1000R and can be found on a black and silver label on the rear door.  The Craftsman mowers' model number is 900.370520 and can be found on a black and silver label on the rear door.

If you have one of these lawnmowers, immedialy stop using and contact Black & Decker or sears for a free inspection.

Circuit Breakers Recalled Due to Fire Hazard

Siemens and Murray issued a voluntary recall of circuit breakers yesterday.  About 2.2 million were produced.  The circuit breakers' spring clip can break easily causing the temperature around the device to rise leading to a fire, personal injury or property damage. 

The circuit breakers, meter combos and load centers being recalled are single and double pole 15 to 50 AMP produced by Siemens and Murray.  Catalog numbers and date codes, 0610 or 0710, are printed on a label on the side of the device.  The product was sold at Lowes, The Home Depot amoung other hardware stores. 

If you suffered an injury due to the device, please report it to CPSC.

The issued devices have these date codes and catalog numbers printed on an inside label:

Product	Date Codes	Catalog Numbers
Circuit Breakers	0610, 0710	Q115, Q120, Q130, Q215, Q230, Q250, MP115, MP115U, MP120, MP130, MP215, MP230, MP230U, MP250
Load Centers	Jun 23 2010 – Aug 25 2010	G2020B1100CP, G3030B1100CP, G4040B1200CUSGP, LC4040B1200P, G3040B1200CP, G3040L1200CP, G4040B1200CP, G3030B1150CP, W3040B1200CP, G1624L1125CP, W4040B1200CP
Meter Combo	Jun 23 2010 – Aug 25 2010	JA2040B1200SP

ASR Hip Implant Recalled

DePuy, a subsidiary of Johnson and Johnson, recalled two DePuy ASR hip replacement systems.  The reason behind the recall is an exceptionally high failure rate leading to patients experiencing pain.  Many of these patients needed revision surgery and a second hip replacement as a result. 

Although the FDA announced the recall in early August, DePuy did not issue a press release until the end of the month.  In the release, they gave detailed information, including that 93,000 devices were sold.  DePuy also suggested patients with their hip implant see a surgeon for evaluation, regardless of if they're experiencing pain or not. 

The DePuy ASR has been on the market since 2005.  Health care professionals have warned the public about the dangers of metal-on-metal hip implants like the ASR.  Such implants can shed metal particles, releasing them into the body and damaging soft tissue.

In the last couple months, a number of lawsuits have been filed against DePuy.

Painful Side Effects Caused by Artimplant Artelon Spacer

The Artimplant Artelon Spacer is a medical device used for people with thumb disabilities.  The product is produced by Artimplant AB and distributed by Small Bone Innovations.  Neither company offers consumers a warning about the multiple reports of painful side effects and other negative, sometimes severe, reactions.

Artimplant Artelon Spacers are surgically implanted into a person’s hand with the intent to relieve arthritis but keep pinch strength intact.  The device itself is made of a mixture of biodegradable and non biodegradable materials.  The biodegradable part works as “scaffolding” in the patient’s hand.  It will take at least six years for the material to completely degrade, meanwhile tissue is supposed to regenerate in the hand. 

However, as is well known among medical professionals, when a foreign object is placed in the body, the body can reject it and react badly to the implanted device.  Many patients have reported serious reactions including loss of motion, swelling and inflammatory synovitis leading to incredible pain.  The Artelon Spacer can also break in the body.  Occasionally, under stress, it has fragmented leaving tiny pieces in the hand, which can cause pain.

The companies behind the Artelon Spacer did minimal investigation and research into the materials used in the device.  In fact, there was just one pilot study, which evaluated only 10 patients.  The study itself was biased, as it was funded by the industry. 

Fun Stuff Recalls Toy Due to Choking Hazard

Fun Stuff Inc. has issued a voluntary recall of the following products:  BoBo Balls (item number FS1814), Klick Klick Balls (item number FS1734) and Click Armband Bracelets (FS1842).  The toys have a small ball at the end which can detach.  Young children could potentially choke on the detached ball. 

The toys feature an armband with balls attached.  They're made of hard plastic and stretchy rubber material with colorful balls (came in purple, blue, green, orange and pink).  The BoBo Balls version included flashing lighted balls.

The product was sold between January 2009 and August 2010 at beach resort stores for $2 to $5.

If your child has one of these toys, immediately take it away.  If your child received an injury from the product, contact CPSC.

The Dangers of Yaz Birth Control

In 2006, Yaz birth control was released.  It is prescribed to be taken orally and daily.  It differs from other birth control pills as it contains drospirenone, a progestin hormone.  Drospirenone increases levels of potassium in the taker's bloodstream.

However, Yaz is linked to many serious side effects including gall bladder disease, stroke, blood clots and heart attack.  The FDA explains, "Yaz has additional risks because it contains the progestin, drospirenone [that] can lead to hyperkalemia in high risk patients, which may result in potentially serious heart and health problems."  The FDA warns women to be aware of not only the risks of this particular birth control but oral contraceptives in general.

Studies have found a link between Yaz and hyperkalemia, a condition where the person has abnormal levels of potassium in the bloodstream.  Such a condition can lead to fatal arrhythmias. 

All oral contraceptives increase a person's risk of heart attack, especially for smokers.  Researchers have also found a link to blood clots and strokes. 

Joseph L. Messa at American AAOS Annual Conference

Founding attorney, Joseph L. Messa, Jr. of Messa & Associates, P.C., recently took part in a symposium at the American Academy of Orthopedic Surgeons (AAOS) annual conference in New Orleans, La.
The program titled, “Beyond Medical Liability Reform: Keeping Our House in Order,” brought to the attention how the prospect of National tort reform has faded since 2006, and most changes and reforms have progressed on a state-by-state basis. However, there have been important changes in the scrutiny being applied to expert witness testimony on both sides, and controversy continues between physicians who act as experts for Plaintiffs and those who defend physicians.

Messa was one of five lecturers, two attorneys (one Plaintiff and one Defense) and three medical doctors (two orthopedic surgeons and one neurosurgeon), who discussed fair and just ways to protect the rights of the harmed patient and improve the safety of medical care all within the economy of sustainable medicine.
Messa discussed the importance of the Physician’s moral and ethical duty to injured patients when an expert witness is needed in court. He believes that, “there is a peer pressure/stigma of testifying for injured patients against other Doctors that make it difficult for legitimately injured patients to make their claims.”
He adds, “As a citizen and as a professional with special training and experience, the physician has an ethical obligation to assist in the administration of justice […] the public should know they will be protected in the event of injury from substandard care."

For more information regarding the symposium, please contact Tina Lumbis at 1-877 MESSALAW or TLumbis@messalaw.com.

Black & Decker Recalls Sanders

Last Thursday, Black & Decker and the US Consumer Product Safety Commission announced the voluntary recall of Black & Decker Random Orbit Sanders.  The platen, a black plastic disk which holds the sandpaper, can break or fly off during use posing a risk to users and anyone nearby.

There have been 73 reports to Black & Decker of incidents where the platen fell apart or broke.  Fifteen of those reports included injuries and one person suffered a serious facial laceration.

The Random Orbit Sanders being recalled are orange and black with model numbers FS3000ROS, RO400, RO410, RO400G, RO410K and RO410LW.  The date codes fall between 200701 and 200929. Each product features "Black & Decker" printed on it and the model number printed on the label.  Users can find the date code on the underside.

The device was sold across the country for $40 between January 2007 and July 2009.  They were sold at hardware, discount and home center stores as well as other authorized Black & Decker dealers.

Owners of the Black & Decker Random Orbit Sander should immediately stop using the device and contact the company for a replacement piece.  Consumers should also report any injuries to the US Consumer Product Safety Commission.

Jo-Ann Fabric Recalls Roll Up Blinds

In December 2009, craft stores began voluntarily recalling roman shades and roll up blinds.  Jo-Ann Fabric announced they are joining the other stores in the recall. 

The recalled product is Bamboo Roll-up Blinds with Valance.  The blinds could potentially strangle a child.  The lifting loop can detach from the side of the blind allowing a child's neck to become entangled. 

The blinds, 36"x72" and 48"x72", were sold at Jo-Ann Fabric and other craft stores across the country for $25 and $30 respectively.  They were available between April and December 2009.  

Wading Staffs Recalled

Simms Fishing Products have announced the voluntary recall of their Wading Staffs, which can collapse and cause users to fall. 

The Wading Staffs were sold at authorized Simms dealers across the country for $120 between March and June 2010.  The staffs are used to assist fishers wading in streams and rivers.  The wading staff was sold in both a 52” and 56” size.  They’re sterling silver with the item numbers AWS101152 or AWS101156 and UPC numbers 94264-10102 or 94264-10103.  These numbers were located on the product hang tag when purchased.  However, the defective products are easily identified by a silver cable connector.

If you purchased the recalled wading staff from Simms Fishing Products, immediately stop using it and contact Simms.  Please report any injuries to the US Consumer Product Safety Commission.

Fingerstick Devices Could Pose Health Risk

The FDA and CDC recently released information regarding fingerstick devices used by health professionals to get small blood specimens. They’re used primarily to test for hemoglobin, blood glucose and other blood components. Over the past 10 to 15 years, the FDA and CDC noticed an increase in the number of bloodborne infection transmissions. These infections, specifically hepatitis B, were caused by point of care (POC) and fingerstick blood testing devices.

The FDA and CDC have warned the health care industry about this threat. POC and fingerstick blood testing devices should not be used on more than one patient for multiple reasons, including the risk of improper use leading to contaminating the lancet blade. Even if the devices are thoroughly cleaned, it is very hard to remove all the blood. Blood left on the device can lead to bloodborne pathogen transmission between patients.

Healthcare professionals are advised to not use fingerstick or POC devices on more than one patient. In some cases, it is not possible to use a POC on only one patient. In which case, the device should be thoroughly cleaned according to the labeling. Healthcare professions and patients are asked to report side effects or adverse results caused by these products to the FDA’s MedWatch Safety Information and Adverse Event Reporting Program.

Sharp LCD TV Recall

Although there has not been a reported injury, Sharp Electronics Corporation is voluntarily recalling their 32 inch LCD TVs. The TV’s stand’s neck can break, which would cause the TV to fall over and possibly injure the consumer.

The TV was sold by a variety of major retailers for around $550 between March and August 2010. The Sharp 32 inch LCD TV’s model number is LC-32SB28UT and can have any of following serial numbers printed on a back label: 0028 32837 through 0028 35190, 0048 57501 through 0048 59020, 0048 61401 through 0048 64020 or 0048 72001 through 0048 78800.

If you purchased a Sharp 32 inch LCD TV, immediately stop using it and contact Sharp for a free replacement piece.

Tygacil, an Intravenous Antibacterial, Poses Higher Mortality Risk

The FDA informed healthcare professionals that the intravenous antibacterial Tygacil (tigecycline) poses a higher mortality risk compared to other drugs used to treat serious infections in a similar manner.

The increased risk was found when clinical trials were analyzed. The exact cause of the deaths was often uncertain, though it was believed to be due to the severe infections worsening. The higher risk of death was most evident, but not limited to, patients treated for pneumonia acquired in the hospital. Other incidents of increased risk include patients treated for skin, diabetic foot and intra-abdominal infections.

Although Tygacil is approved by the FDA for treating community acquired pneumonia, skin structure and complicated skin infections and complicated intra-abdominal infections it is not FDA approved for treating diabetic foot infection or hospital-acquired pneumonia.

The FDA notified healthcare professionals of these high risks through a Dear Health Care Professional letter. They also updated the Adverse Reactions and Warnings and Precautions sections on the Tygacil label.

Slow Cookers, sold at Kohl’s Department Store, Recalled

Bella Kitchen’s 5 quart programmable slow cookers have been recalled. The slow cookers were sold exclusively at Kohl’s Department Store with the model number WJ-5000DE and either date code 0907 or 0909. The devices are black with “Bella Kitchen” on the control panel and the model number and date code on a label underneath the slow cooker.

The panel of the slow cooker can overheat and melt, which creates a risk of fire. There have been 60 reports of the device melting, smoking or sparking and three reported incidents of the device catching fire. To date, there has been damage to countertops but no reported injuries.

Kohl’s Department store sold the slow cookers, distributed by Sensio Inc, between July and December 2009 for $20 to $40. If you have this product, immediately unplug and stop using it. Contact Sensio for a refund.

Cargill Meat Solutions Corp Recalls 8,500 Lbs of Ground Beef

Cargill Meat Solutions Corp—located in Wyalusing, PA—is recalling 8,500 pounds of ground beef because of possible E. coli 026 contamination. As reported by the Food Safety and Inspection Service, this is a Class I recall with a high health risk.

The recalled product is a 42 pound case of “Ground Beef Fine 90/10,” use/freeze by date 7/1/10, establishment number EST 9400 and product code W69032. The beef was eventually repackaged and sold as smaller, consumer sized packages

The ground beef, produced on June 11, was initially distributed to Maryland and Connecticut but was distributed elsewhere since. E. Coli 026 related illnesses have been reported in Main and New York. FSIS has determined the recalled ground beef from Cargill Meat Solutions is directly related to these incidents.

The bacteria E. Coli can cause dehydration, bloody diarrhea and, in severe cases, kidney failure.

Iams, Eukanuba Pet Food Recall

Procter & Gamble is expanding a dog and cat food recall to include veterinary and some specialized dry pet food as a precautionary measure because there is the possibility of salmonella contamination. Though it should be emphasized that no salmonella-related illnesses have been reported.

The following dry pet food products are included in the recall:

Iams Veterinary Dry Formulas

Eukanuba Naturally Wild

Eukanuba Pure

Eukanuba Custom Care Sensitive Skin

For a full list consult the Iams website. The affected products are sold in veterinary clinics and specialty pet retailers throughout the United States and Canada. No canned food, biscuits/treats or supplements are affected by this announcement. A full listing of UPC codes can be found at the Iams site.

These products are made in a single, specialized facility. In consulation with the Food and Drug Administration, P&G decided to recall all foods made at that facility.

The company advises consumers who have purchased the specific dry pet foods listed should discard them. People handling dry pet food can become infected with salmonella, especially if they have not thoroughly washed their hands after having contact with surfaces exposed to this product. Symptoms of salmonella poisoning include nausea, vomiting, diarrhea, abdominal cramping and fever. Rarely, salmonella can result in more serious ailments including arterial infections, endocarditis, arthritis, muscle pain, eye irritation and urinary tract symptoms.

Pets with salmonella infections may have decreased appetite, fever and abdominal pain. If left untreated, pets may be lethargic and have diarrhea or bloody diarrhea, fever and vomiting. Infected but otherwise healthy pets can be carriers and infect other animals or humans. If your pet has consumed the recalled product and has these symptoms, please contact your veterinarian.

Husqvarna Lawn Tractor Recall: Fire Danger

Husqvarna is recalling a series of riding lawn tractors sold this year after getting more than 50 complaints of damaged fuel lines, something that could cause a fire, the U.S. Consumer Product Safety Commission said.

The CPSC said the fuel line to the rear-mounted fuel tank is too long and can get damaged by moving parts when the tractor is in use. Those who have the lawn tractors are urged to stop using them until a free repair can be arranged by Husqvarna.

No injuries have been cited in the 53 reports of fuel-line damage received by Husqvarna.

Husqvarna said it has sold about 1,700 of the gas-powered tractors, which are designed for residential use. The tractor being recalled is the GTH27V52LS with model numbers 96043009100 and 96043009900 and serial numbers 010810A00XXXX through 05061000XXXX.

For more information, please call 1877 MESSALAW.

Toyota Recalls over 400,000 Vehicles over Steering Issues

Toyota Motor Corp. said Thursday it was recalling more than 400,000 older-model vehicles sold in the United States, citing potential steering-related problems in both.

The Japanese automaker said the recall would affect 373,000 Toyota Avalon’s manufactured between 2000 to 2004. The company said the vehicle's steering lock bar could break under certain conditions, increasing the risk of a crash.

Toyota also cited steering issues in its recall of some 39,000 Lexus LX 470 vehicles. The company said that if the vehicle experienced a severe impact to the front wheels, such as striking a pothole, the steering shaft could disengage over time. The recall only affects vehicles from model years 2003 to 2007.

The company said it was not aware of any accidents related to its Lexus LX 470.

The company said it would begin to send out notifications in mid-August to owners of the vehicles affected by Thursday's recall. Drivers will be able to bring their car to a local dealer to have the vehicle fixed at no charge.

For more information, please call 1877 MESSALAW.

30,000 Nap Nanny Baby Recliners Recalled after Baby Dies

Nap Nanny Baby recliners are being recalled after a 4 month-old Michigan girl was found dead in one. She was in the harness on the recliner but was found hanging over the side, stuck between a crib bumper and the Nap Nanny.

Baby Matters, who makes Nap Nanny, said over 30,000 of the recliners will be a part of the recall. The recliners were made in China and sold nationwide for about $130.

The U.S. Consumer Product Safety Commission said that there has been over 21 other incidents involving the product that have been reported, mostly with infants younger than five months falling over the side.

Anyone with a Nap Nanny is asked to stop using it immediately.

1 Million Shades & Blinds Recalled

Smith + Noble has issued a recall for more than 1 million shades and blinds after a boy nearly strangled in Washington State.

The recall includes all custom Roman shades from the company as well as roller shades without a tension device on the cord. The shades were sold under the following brands:

Smith + Noble, Christopher Lowell, Jessit Gold, Shop Blinds, & Window Elements.

Tens of millions of shades have been recalled in the past year as a part of a major industry initiative to help prevent the strangulation deaths of children. Children can strangle in the cords on the back of the shades and in the loop of the roller shades.

Consumers are asked to stop using the shades until they obtain a repair kit which they can get by calling the Window Covering Safety Council at (800) 228-7638.

GSK Agrees to $460 Million Avandia Settlement

GlaxoSmithKline (GSK) agreed to settle 10,000 lawsuits alleging that its popular diabetes drug Avandia injured patients.

The settlements come as the Food and Drug Administration (FDA) begins two days of hearings into the safety of the drug. Earlier today, documents were released that suggested GSK hid data that showed Avandia increased the risk of heart attacks, heart failure and strokes.

For more information please contact 1877 MESSALAW.

Avandia Heart Risks Buried by Drug Company

The pharmacy company that makes the popular diabetes drug Avandia, SmithKline Beecham, knew for over a decade that the drug caused an increased risk of heart problems – but covered up the information according to a report published in the New York Times.

The Times report said that SmithKline did not post results of its drug trial findings on its website or submit them to federal regulators. This information was based on internal company documents it obtained.

According to a March 21, 2001 email the Times obtained, a company executive wrote about the study results:

“This was done for the U.S. business, way under radar. Per Sr. Mgmt request, these data should not see the light of day to anyone outside of GSK.” (GlaxoSmith Kline is the corporate successor to SmithKline)

Today, FDA panel will begin determining what to do about Avandia. More than half a million Americans have been prescribed Avandia, but the covered up studies issue that the drug have linked it to a raised risk of stroke, heart attack, and even death.

For more information please call 1877 MESSALAW.

BREAKING NEWS: Duck Boat Crash in Philadelphia

A duck boat packed with tourists crashed into a barge on the Delaware River this afternoon soon after it entered the water at Penns Landing, police said.

The collision, at about 2:40 p.m., sent a number of people into the river off Columbus Boulevard. About 40 people were on board the duck boat.

Rescue boats pulled individuals wearing life vests from the water.

Tourists board the boats at Independence Mall and after touring Old City they enter the river for a brief tour at a ramp just south of the Ben Franklin Bridge.

Please call 1877 MESSALAW for more information.

MRSA/SA Test Recalled Because of Rare False-Negative Results

A test to detect methicillin-resistant Staphylococcus aureus (MRSA) and S aureus (SA) has been recalled by the manufacturer based on an increasing number of complaints about false negatives for MRSA.

The voluntary recall of the Xpert MRSA/SA Blood Culture Assay covers all kits made and distributed from October 21, 2008 through June 21, 2010. The kit is manufactured by Cephid which is based in Sunnyvale, California. The product has been distributed to hospital laboratories worldwide.

Because the test has the rare potential to generate false-negative MRSA results, patients with MRSA infections may receive incorrect treatment or delayed care, according to an alert sent by MedWatch (the US Food and Drug Administration (FDA), the FDA's safety information and adverse event reporting program.

Customers can continue to use the product and report results of MRSA positive/SA positive - however, when customers receive a MRSA negative/SA positive result, the company recommends conducting further antimicrobial susceptibility testing using an FDA-cleared method for an accurate MRSA finding.

Customers with questions about the recall can contact the Cepheid Technical Support at 1-888-838-3222.

P&G Recalls 4 Hour Decongestant Nasal Spray in US

The Procter & Gamble Company announced they are voluntarily recalling its 4-Hour Decongestant Nasal Spray. The product was distributed nationwide in the United States.

P&G said it is taking this voluntary precautionary step after finding that the product formulation may not meet the expiration dates on the package. This recall is not a result of consumer complaints.

P&G is removing the product in question from store shelves. Consumers who have product with the UPC codes listed below and marked with an expiration date prior to June 2013 should simply discard the affected product.

The product name is: VapoSpray 4 Hour Nasal Spray by Sinex with a UPC code of 3 23900 00082 7. Prior to June 2009, this product was also sold as Sinex Nasal Spray in both a spray (UPC Code 3 23900 00082 7) and Ultra Fine Mist package (UPC Code 3 23900 00085 8).

For more information, please contact 1877 MESSALAW.

Equate Ibuprofen Recall – Metal Shavings in Bottles

L. Perrigo Co has recalled one lot of Equate Ibuprofen 200 mg tablets packaged in bottles of 100 tablets. These recalled Equate Ibuprofen tablets have lot number 9BE1961 printed on the label or stamped on the bottle. The pills are being recalled because there may be metal shavings in the containers.

L. Perrigo Company is the world’s largest manufacturer of OTC pharmaceutical products for the store brand market. More details involving this recall are below:

PRODUCT

Equate Ibuprofen Tablets, 200 mg, 100 coated Tablets, NDC 49035-604-78. Recall # D-422-2009

CODE

Lot 9BE1961

For more information, please call 1877 MESSALAW.