P&G RECALLS SOME IAMS CAT FOOD

Procter & Gamble (P&G) is voluntarily recalling a small number of bags of its Iams Proactive Health Indoor Weight & Hairball Care dry cat food which may have been sold recently in one or two stores in Loveland, Colorado.

These bags have the potential to contain salmonella, although no illnesses have been reported.  No other Iams pet food products are affected.

The Iams Proactive Health Indoor Weight & Hairball Care cat food in question is sold in blue 6.8-pound bags.  These bags feature a code date of 02304173 (B1-B6) and the UPC number 1901403921.

If you have this product, please discard it and call P&G toll-free for a product replacement at 800-862-3332 Monday-Friday, 9:00 a.m. to 6:00 p.m. EST.

P&G has worked with its retailers to remove the affected product from stores in the area.  P&G believes that only three bags may have been purchased recently by consumers in the area.  Yet, as a precautionary measure, the company is initiating this retrieval.

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.  Healthy people infected with salmonella should monitor themselves for some or all of the following symptoms: nausea, vomiting, diarrhea or bloody 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. Consumers exhibiting these signs after having contact with this product should contact their healthcare providers.

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.

CARGILL RECALLS GROUND BEEF - ECOLI SCARE

Cargill recalled 8,500 pounds of ground beef late Friday that may contain E coli.

"The move came after three people, two in Maine and one in New York, were identified as becoming ill from a strain of E. coli," CNN said, citing a government statement. "The USDA says it believes certain BJ's Wholesale Club stores in Connecticut, Maine, Maryland, Massachusetts, New Hampshire, New Jersey, New York and Virginia received the products," the news service added.

Cargill is one of the largest companies in the U.S., with annual revenue of $108 billion and net income of $2.6 billion.

WILLIAMS-SONOMA RECALLS BABY BOTTLE WARMERS

WASHINGTON, D.C. - The U.S. Consumer Product Safety Commission, in cooperation with the firm named below, today announced a voluntary recall of the following consumer product. Consumers should stop using recalled products immediately unless otherwise instructed. It is illegal to resell or attempt to resell a recalled consumer product.

Name of Product: Beaba Express Steam Bottle Warmers

Units: About 11,000

Importer: Williams-Sonoma Inc., of San Francisco, Calif.

Hazard: The bottle warmers can overheat liquids and baby food, posing a burn hazard to adults and babies.

Incidents/Injuries: The firm has received 10 reports of the bottles overheating, including one report of an adult who received a finger burn from touching a hot bottle.

Description: This recall involves the Beaba Express Steam Bottle Warmer which uses steam to heat baby bottles or baby food. The bottle warmer is green with an orange temperature dial. "Beaba" is printed on the base and model number 9602 is printed on the underside of the warmer.

Sold at: Williams-Sonoma stores nationwide, online at www.williams-sonoma.com and through Williams-Sonoma catalogs from June 2010 through July 2010 for about $65.

Manufactured in: China

Remedy: Consumers should immediately stop using the recalled bottle warmers and call Williams-Sonoma for instructions on how to return the product for a full refund. Additionally, consumers who return the bottle warmers will receive a $25 Williams-Sonoma merchandise card.

Consumer Contact: For additional information, contact Williams-Sonoma toll-free at (877) 548-0850 between 4 a.m. and 9 p.m. PT seven days a week or visit the firm's website at www.williams-sonoma.com

CHAR-BROIL RECALLS VERTICAL GAS SMOKERS

WASHINGTON, D.C. - The U.S. Consumer Product Safety Commission, in cooperation with the firm named below, today announced a voluntary recall of the following consumer product. Consumers should stop using recalled products immediately unless otherwise instructed. It is illegal to resell or attempt to resell a recalled consumer product.

Name of Product: Char-Broil vertical gas smokers

Units: About 18,450

Importer: Char-Broil LLC, of Columbus, Ga.

Manufacturer: Ningbo Spring Communications of China

Hazard: When the temperature setting is in "low," the smoker's hose/valve/regulator (HVR) assembly does not allow sufficient gas to flow, causing the flame to extinguish. Gas continues to flow and build up inside the smoker. If the smoker is reignited the build-up of propane gas can cause an explosion that bursts the smoker's door open, posing an injury hazard.

Incidents/Injuries: The company has received five reports of doors bursting open and hitting consumers. Injuries reported include burns to face and head, head concussion and cuts.

Description: This recall involves the Char-Broil vertical gas smokers with model number 07701413. The model number is printed on a metal tag located on the right rear leg of the smoker. The smoker measures 21.5" x 19.5" x 45.5" and weighs 75 pounds. A "G" inside a triangle is printed on the regulator (see photo).

Sold at: Walmart and various other retailers nationwide from March 2008 through June 2010 for about $140.

Manufactured in: China

Remedy: Consumers should stop using the recalled smokers and contact Char-Broil for a free replacement hose/valve/regulator assembly and installation instructions.

Consumer Contact: For additional information, contact Char-Broil toll-free at (866) 671-7988 between 8 a.m. and 6 p.m. ET Monday through Friday, or visit the firm's website at www.charbroil.com

TELEVISION WALL MOUNTS RECALLED

WASHINGTON, D.C. - The U.S. Consumer Product Safety Commission, in cooperation with the firm named below, today announced a voluntary recall of the following consumer product. Consumers should stop using recalled products immediately unless otherwise instructed. It is illegal to resell or attempt to resell a recalled consumer product.

Name of Product: Flat screen television wall mounts

Units: About 131,000

Manufacturer: Milestone AV Technologies LLC, of Savage, Minn.

Hazard: The elbow joint components on the wall mount’s arm do not fit together properly, causing the attached television to tilt and possibly fall when the television is adjusted. This could pose an injury hazard to a consumer.

Incidents/Injuries: None reported.

Description: This recall involves the Sanus Vision Mount model LF228-B1 wall mounts and Simplicity model SLF2. The wall mounts were sold for flat screen televisions. The model numbers can be found on the UL sticker on the wall plate.

Sold at: The Sanus Vision Mount model LF228-B1 was sold through independent television mount dealers nationwide from June 2009 through July 2010 for about $450. The Simplicity model SLF2 was sold through Costco from June 2009 through July 2010 for about $200.

Manufactured in: China

Remedy: Consumers should immediately inspect the wall mount to determine if the elbow joint fits properly and contact Milestone for a free replacement wall mount arm. Instructions for visual inspections are located at www.milestone.com/recall

Consumer Contact: For additional information, contact Milestone toll-free at (877) 894-6280 between 8 a.m. and 9 p.m. CT Monday through Friday and between 10:30 a.m. and 7 p.m. CT Saturday through Sunday or visit the firm’s website at www.milestone.com/recall

MAGNETIC MAZE BOARDS RECALLED

WASHINGTON, D.C. - The U.S. Consumer Product Safety Commission, in cooperation with the firm named below, today announced a voluntary recall of the following consumer product. Consumers should stop using recalled products immediately unless otherwise instructed. It is illegal to resell or attempt to resell a recalled consumer product.

Name of Product: Magnetic maze boards

Units: About 18,500

Manufacturer: Lakeshore Learning Materials, of Carson, Calif.

Hazard: The magnetic maze board’s plastic wand can separate and expose a magnet that can be a choking hazard to children. Also, if a child has more than one of these toys and the magnets detach and are swallowed, the magnets can attract each other and cause intestinal perforations or blockages, which can be fatal.

Incidents/Injuries: Lakeshore has received ten reports of wands separating and magnets detaching. No injuries have been reported.

Description: This recall involves wooden magnetic maze boards. The wooden boards have a clear plastic sheet that covers small wooden or plastic pieces located inside a maze. A plastic wand containing a magnet in its tip is attached to the board by a cord. The wand is used to move items inside the maze. The top of the board reads: “Who’s Hiding in the Garden?,” “Who’s Hiding in the Ocean?,” “Magnetic Counting Maze,” “Magnetic Alphabet Board” or “My Community Magnetic Board.”

Sold by: Lakeshore Learning Materials stores nationwide, its catalogs and online at www.lakeshorelearning.com from January 2009 through May 2010 singly or in sets for between $30 and $40.

Manufactured in: China

Remedy: Consumers should immediately take this toy away from children and contact Lakeshore to receive a free replacement product.

Consumer Contact: For additional information, contact Lakeshore Learning Materials at (800) 428-4414 between 8 a.m. and 5 p.m. PT Monday through Friday, or visit the company’s website at www.lakeshorelearning.com

NEW AUGUST TOYOTA RECALL:

Toyota Motor Corp. said Thursday it is recalling 1.33 million Corolla sedans and Matrix hatchbacks from the 2005-2008 model years because their engines may stall. Three accidents and one minor injury may be related to the recall.

Toyota has recalled more than 10 million vehicles worldwide over the past year for a range of quality problems. Federal regulators have been investigating the Corolla and Matrix engine issue since December.

Toyota will alert owners and fix the engine problem for free starting in mid-September.

EGG RECALL EXPANDS TO 380 MILLION

Contact:
Egg Safety Media Hotline
404/367-2761
info@eggsafety.org

FOR IMMEDIATE RELEASE - August 18, 2010 - The following statement was released by officials of Wright County Egg regarding the US Food and Drug Administration’s (FDA) investigation of potential incidence of Salmonella enteritidis (SE).

Wright County Egg of Galt, Iowa is expanding its voluntary recall (original recall date: August 13, 2010) of specific Julian dates of shell eggs produced by their farms because they have the potential to be contaminated with Salmonella. Salmonella is an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Healthy persons infected with Salmonella often experience fever, diarrhea, nausea, vomiting and abdominal pain. In rare circumstances, infection with Salmonella can result in the organism getting into the bloodstream and producing more severe illnesses such as arterial infections, endocarditis or arthritis.

Eggs affected by the expanded recall were distributed to food wholesalers, distribution centers and foodservice companies in California, Arizona, Missouri, Minnesota, Texas, Georgia, Washington, Oregon, Colorado, Nevada, Iowa, Illinois, Utah, Nebraska, Arkansas, Wisconsin and Oklahoma. These companies distribute nationwide.

Eggs are packaged under the following brand names: Albertsons, Farm Fresh, James Farms, Glenview, Mountain Dairy, Ralphs, Boomsma, Lund, Kemps and Pacific Coast. Eggs are packed in varying sizes of cartons (6-egg cartons, dozen egg cartons, 18-egg cartons, and loose eggs for institutional use and repackaging) with Julian dates ranging from 136 to 229 and plant numbers 1720 and 1942.

Dates and codes can be found stamped on the end of the egg carton or printed on the case label. The plant number begins with the letter P and then the number. The Julian date follows the plant number, for example: P-1720 223.

Prior Recall
Eggs under the August 13, 2010 recall are packaged under the following brand names: Lucerne, Albertson, Mountain Dairy, Ralph’s, Boomsma’s, Sunshine, Hillandale, Trafficanda, Farm Fresh, Shoreland, Lund, Dutch Farms and Kemps. Eggs are packed in varying sizes of cartons (6-egg cartons, dozen egg cartons, 18-egg cartons, and loose eggs for institutional use and repackaging) with Julian dates ranging from 136 to 225 and plant numbers 1026, 1413 and 1946.

There have been confirmed Salmonella enteritidis illnesses relating to the shell eggs and traceback investigations are ongoing.

Wright County Egg is fully cooperating with FDA’s investigation by undertaking this voluntary recall. Our primary concern is keeping Salmonella out of the food supply and away from consumers. As a precautionary measure, Wright County Egg also has decided to divert its existing inventory of shell eggs from the recalled plants to a breaker, where they will be pasteurized to kill any Salmonella bacteria present.

Consumers who believe they may have purchased these shell eggs should not eat them but should return them to the store where they were purchased for a full refund. This recall is of shell eggs only. Other egg products produced by Wright County Eggs are not affected. Consumers with questions should visit www.eggsafety.org⁹ or call Wright County’s toll-free information number (866-272-5582), which contains a message outlining recall instructions for consumers.

We are undertaking this additional recall to further protect the safety of consumers - this voluntary measure is consistent with our commitment to egg safety, and it is our responsibility.

DOUBLE STROLLERS RECALLED: COLLAPSE HAZARD

WASHINGTON, D.C. - The U.S. Consumer Product Safety Commission, in cooperation with the firm named below, today announced a voluntary recall of the following consumer product. Consumers should stop using recalled products immediately unless otherwise instructed. It is illegal to resell or attempt to resell a recalled consumer product.

Name of Product: Double stroller

Units: About 3,700

Distributor: Lan Enterprises LLC of Hillsboro, Ore., and formerly of Beaverton, Ore.

Hazard: The stroller's frame latch above the front wheels can fail when the stroller hits an object, causing the stroller to unexpectedly collapse. This can result in minor scrapes, cuts and bruises.

Incidents/Injuries: The company has received 185 reports of frame latch failures. In one incident a 13-month-old boy and a 3-year-old boy received scrapes and bruises when their stroller hit a sidewalk and the stroller collapsed.

Description: This recall involves 2007 and 2008 Zooper Tango double strollers with a model number of SL808B and SL808F. The model numbers were printed on the original packaging. The strollers have production dates ranging from January 1, 2007, through April 30, 2008. The production dates are printed on the warning labels attached to the seats. The word "Zooper" is printed on the stroller canopies and grab bars. The Web address www.zooper.com is printed on the basket under the stroller seats.

Sold at: Juvenile product and mass merchandise retailers nationwide and at www.babiesrus.com from January 2007 through August 2008 for between $400 and $430.

Manufactured in: China

Remedy: Consumers should immediately stop using these recalled strollers and contact Zooper USA to receive a free repair kit.

Consumer Contact: For additional information, contact Zooper USA toll-free at (888) 966-7379 between 9 a.m. and 5 p.m. PT Monday through Friday or visit the firm's website at www.zooper.com

ELECTRICAL WIRE RECALLED DUE TO FIRE HAZARD

WASHINGTON, D.C. - The U.S. Consumer Product Safety Commission, in cooperation with the firm named below, today announced a voluntary recall of the following consumer product. Consumers should stop using recalled products immediately unless otherwise instructed. It is illegal to resell or attempt to resell a recalled consumer product.

Name of Product: THHN Electrical Wire

Units: About 1,000

Manufacturer: Cerro Wire Inc., of Crothersville, Ind.

Hazard: While the actual electrical wire has “14 gauge” printed on it, the packaging incorrectly labels the electrical wire as 12 gauge. If used as a 12 gauge wire, it can overload, posing a fire hazard to consumers.

Incidents/Injuries: None reported.

Description: This recall involves THNN electrical wire labeled on its packaging as 12 gauge solid white 100’ UPC 48243982721 and 12 gauge stranded red 50’ UPC 48243229215. The actual wire has “THHN Cerro Wire 14 gauge” printed on it. The UPC number and 12 gauge is found on the plastic wrap and on a label at the bottom of the reel.

Sold at: Home Depot & Menards stores in the following states: Colo., Iowa, Idaho, Ill., Ind., Kan., Ky., Mich., Minn., Mo., Mont., N.D., Neb., Ohio, Ore., Pa., S.D., Utah, Wash., Wis., Wyo. from December 2009 through April 2010. The 50-foot wire spools were sold for $9 and the 100-foot spools for about $16.

Manufactured in: United States

Remedy: Consumers should immediately stop using any switches, outlets or electrical devices using this wire and contact Cerro Wire for instructions on returning the product for a refund. Any contractor or subcontractor who used this wire should inspect their work to see that their work meets local electrical wiring code.

Consumer Contact: For additional information, contact Cerro Wire toll-free at (866) 572-3776 ext. 269 between 7 a.m. and 5 p.m. ET Monday through Friday or visit the firm’s website at www.cerrowire.com

POTTERY BARN KIDS RECALLS BUNK BEDS - ENTRAPMENT HAZARD

WASHINGTON, D.C. - The U.S. Consumer Product Safety Commission, in cooperation with the firm named below, today announced a voluntary recall of the following consumer product. Consumers should stop using recalled products immediately unless otherwise instructed. It is illegal to resell or attempt to resell a recalled consumer product.

Name of Product: Bunk Beds

Units: About 405

Importer/ Distributor: Pottery Barn Kids, a division of Williams-Sonoma, Inc., of San Francisco, Calif.

Hazard: The end structure of the bunk bed can pose an entrapment hazard to young children, a violation of the Safety Standard for Entrapment Hazards in Bunk Beds, 16 C.F.R. Part 1513. Children can get their necks caught in the opening between the post and the decorative molding.

Incidents/Injuries: None reported.

Description: This recall involves Madeline bunk beds. The bed is white and is made of wood and medium-density fiberboard. It has guardrails on either side of the top bunk and a ladder that attaches to the side of the beds.

Sold at: Pottery Barn Kids stores, catalog and www.potterybarnkids.com from July 2009 to March 2010 for $1,400

Manufactured in: Vietnam

Remedy: Consumers should immediately stop using the bed and contact Pottery Barn Kids to schedule installation of a free repair kit.

Consumer Contact: For additional information, contact Pottery Barn Kids toll-free at (888) 779-8692 between 7 a.m. and midnight PT seven days a week or visit the company's website at www.potterybarnkids.com

COUNTERFEIT BLACKBERRY BATTERIES RECALLED -- BURN HAZARD

Name of Product: Counterfeit BlackBerry®-branded cell phone batteries in refurbished devices

Units: About 470,000

Distributor: Asurion, of Smyrna, Tenn.

Hazard: The counterfeit batteries can overheat, posing burn and fire hazards.

Incidents/Injuries: Asurion has received two reports of counterfeit BlackBerry®-branded batteries overheating, causing minor burns to a consumer's finger and minor property damage to a sofa and car seat.

Description: This recall involves only BlackBerry®-branded batteries provided with refurbished Blackberry®-branded devices. The refurbished devices were sent to consumers by Asurion through a handset protection program. The batteries were used across virtually all models of refurbished BlackBerry devices distributed by Asurion prior to November 1, 2009. Genuine Blackberry-branded batteries are not included in this recall. No other Asurion or BlackBerry products are involved in this recall.

Distributed through: Asurion as part of their handset protection claim program nationwide from March 2004 through October 2009.

Manufactured in: Unknown

Remedy: Consumers who received refurbished BlackBerry devices through Asurion prior to November 1, 2009 should immediately stop using the product and contact Asurion for a replacement product. Asurion is directly contacting known consumers with the affected batteries to notify them of this recall.

Consumer Contact: For more information, contact Asurion toll-free at (866) 384-9175 between 8 a.m. and 7 p.m. CT Monday through Friday, or visit the firm's website at www.001batex.com

REPAIR LEVERAGE GYMS RECALLED BECAUSE OF INJURY RISK

The following product safety recall was voluntarily conducted by the firm in cooperation with the CPSC and Health Canada. Consumers should stop using the product immediately unless otherwise instructed. It is illegal to resell or attempt to resell a recalled consumer product.

Name of product: Leverage Gyms

Units: About 1,000

Manufacturer: Powertec, of Carson, Calif.

Hazard: Detachment of the exercise workbench from the gym system causes instability, posing a risk of injury to consumers.

Incidents/Injuries: No injuries have been reported.

Description: This recall involves the Workbench Leverage Gym, 2010 version, which has a lock and load removable bench section opening up the lever area for power exercises such as squats, shrugs and rows. The gym has black upholstery and either a black or yellow frame. The Powertec logo with the Workbench series name is printed on the removable bench. The models affected by this recall are WB-LS10 and WB-LS10-B. . Workbench Levergyms™ with model numbers WB-LS10 and WB-LS10B sold after February 2010 are not affected by this recall.

Sold by: Fitness equipment dealers nationwide and online at www.powertecfitness.com from October 2009 through February 2010 for about $850.

Manufactured in: China

Remedy: Customers should immediately stop using the product and contact Powertec to receive a free repair kit or to schedule a free repair with an authorized dealer. The firm has contacted all known purchasers of this product.

Consumer Contact: For additional information, call Powertec toll-free at (877) 525-5710 between 7:30 a.m. and 3:30 p.m. PT Monday through Friday, email the firm at info@powertecfitness.com or visit the firm's website at www.powertecfitness.com

Note: Health Canada's press release is available at http://cpsr-rspc.hc-sc.gc.ca/PR-RP/recall-retrait-eng.jsp?re_id=1142

BABY MONITORS RECALLED BECAUSE OF OVERHEATING

WASHINGTON, D.C. - The U.S. Consumer Product Safety Commission, in cooperation with the firm named below, today announced a voluntary recall of the following consumer product. Consumers should stop using recalled products immediately unless otherwise instructed. It is illegal to resell or attempt to resell a recalled consumer product.

Name of Product: Levana Wireless Video Baby Monitors

Units: About 800

Distributor: Circus World Displays Limited (CWD), of Niagara Falls, Ontario, Canada.

Hazard: Wiring in the baby monitor camera can overheat and emit smoke, posing a burn hazard to consumers.

Incidents/Injuries: Circus World Displays has received two reports of the camera portion of the monitors overheating and smoking. No injuries have been reported.

Description: This recall involves Levana wireless baby monitors with model number LV-TW300. The receiver front is white and green with six round buttons and the printed word "Levana". It is 7 inches tall and includes a stand/base. The camera is all white, about 5 inches tall and is attached to a 3 1/2 inch long white base. The camera can rotate and swivel in various directions. The camera and receiver each has its own A/C adapter.

Sold at: BB Buggy and Health and Safety stores nationwide and on the Internet between February 2010 and May 2010 for about $200.

Manufactured in: China

Remedy: Consumers should immediately stop using and return the baby monitor directly to CWD for a refund or replacement with a different model. When returning, please include the entire product, your complete name, mailing address and phone number in the package and mail to Circus World Displays Ltd, Attention: Adam Crysler, Dealer Returns Specialist, 60 Industrial Parkway Suite Z64, Cheektowaga, NY 14227

Consumer Contact: For additional information, contact Circus World Displays toll-free at (866) 946-7828 between 8 a.m. and 5 p.m. ET Monday through Friday, by e-mail at support@svat.com or on the firm's website at www.mylevana.com

SALAD RECALL BECAUSE OF LISTERIA

SALINAS, California (USFDA) -- Fresh Express is voluntarily recalling 2,825 cases of Veggie Lovers Salad with a Product Code of I208 and Use-by Date of August 10, 2010 out of an abundance of caution due to a possible health risk from Listeria monocytogenes. No other Fresh Express salads are included in the recall. No illnesses have been reported in association with the recall.

Only the Veggie Lovers salad products with a Product Code of I208 and a Use-by Date of August 10 are included in the recall. Retailers and Consumers who have any remaining product should not consume it, but rather discard it. Retailers and Consumers with questions may call the Fresh Express Consumer Response Center at (800) 242-5472, Monday – Friday, 5 a.m. – 8 p.m., Pacific Time. Consumers can find the Product Code and Use-by Date in the upper right-hand corner of the package.

This precautionary recall is being conducted to reach retailers as well as consumers. Consumers should check their refrigerators for Fresh Express Veggie Lovers salad with a Product Code of I208 and a Use-by Dates of August 10, 2010. If they have the product, they should immediately discard it. Retailers should check their inventories and store shelves to confirm that none of the product is mistakenly present or available for purchase by consumers or in warehouse inventories. Fresh Express customer service representatives are already contacting retailers and are in the process of confirming that the recalled product is not in the stream of commerce. Although limited in number, the cases were distributed by Fresh Express to 13 states with the potential for redistribution by customers to an additional 14 states (see listing).

Listeria monocytogenes is a bacterium that can cause foodborne illness in a person who eats a food item contaminated with it. Symptoms of infection may include fever, muscle aches, gastrointestinal symptoms such as nausea or diarrhea. If it spreads to the nervous system symptoms may include headache, stiff neck or confusion. The illness primarily impacts pregnant women and adults with weakened immune systems. Most healthy adults and children rarely become seriously ill.

The precautionary recall notification is being issued due to an isolated instance in which one package of Fresh Express Veggie Lovers Salad yielded a positive result for Listeria monocytogenes in a random sample test collected and conducted by the Ohio Department of Agriculture.

Fresh Express is coordinating closely with regulatory officials. Immediately upon learning about the positive test result, Fresh Express conducted a traceability assessment and a full review of its food safety documentation, all of which were found to be in compliance and were negative for the presence of any bacteria.

- States Distributed: MO, MI, OH, IL, WI, IN, MD, MA, NY, KS, KY, PA, NJ

- Possible Redistribution States: AR, TN, WV, IA, MN, DC, VA, VT, NH, NE, RI, PA, CT, MS

TWEEN BRANDS RECALLS CHILDRENS METAL JEWELRY

WASHINGTON, D.C. - The U.S. Consumer Product Safety Commission, in cooperation with the firm named below, today announced a voluntary recall of the following consumer product. Consumers should stop using recalled products immediately unless otherwise instructed. It is illegal to resell or attempt to resell a recalled consumer product.

Name of Product: Metal Necklaces, Bracelets and Earrings

Units: About 137,000

Importer/Distributor: Tween Brands Inc., of New Albany, Ohio

Hazard: The children's metal jewelry contains high levels of cadmium. Cadmium is toxic if ingested by children and can cause adverse health effects.

Incidents/Injuries: None reported

Description: This recall involves 19 different styles of children's metal necklaces, bracelets and earrings. Styles and shapes of the jewelry include hearts, heart locks, butterflies, cupcakes, peace signs and crowns. Some jewelry contains the words "Best," "Friends" or "Forever" and/or "BFF." Only style numbers listed below are included in this recall. The style number is included on the jewelry's packaging.

Johnson & Johnson Unit Recalls More OTC Products

NEW YORK (AP) -- Johnson & Johnson said Thursday it is expanding a recall of over-the-counter drugs including Tylenol and Motrin IB because of a musty or moldy smell.

The McNeil Consumer Healthcare business said it is recalling 21 lots of over-the-counter drugs sold in the U.S., Puerto Rico, Fiji, Guatemala, the Dominican Republic, Trinidad and Tobago, and Jamaica. The drugs that are being recalled include Benadryl, Children's Tylenol, Motrin IB, Tylenol Extra Strength, Tylenol Day & Night, and Tylenol PM.

The New Brunswick, N.J., company has already made a large recall of those drugs and over-the-counter products, saying about 70 people noticed the smell. Some of them got sick, with symptoms including nausea, stomach pain, vomiting and diarrhea. The odor was linked to a chemical in shipping pallets and traced to a facility in Puerto Rico.

The company had planned to stop shipping those products on wooden pallets treated with the chemical, and asked its suppliers to do the same.

Johnson & Johnson said the latest recall applies to products made before the January recall.

The world's biggest maker of health care products, Johnson & Johnson enjoyed a strong reputation for safety, but it has dealt with several product recalls since late last year. It withdrew over-the-counter drugs in November and December 2009 before issuing a much larger recall in January. Federal regulators said McNeil was told about the problem in early 2008 but made a limited investigation and did not tell the Food and Drug Administration quickly.
The original withdrawal also included other types of Tylenol, Benadryl, Rolaids, Simply Sleep, and St. Joseph's aspirin.

In late April, McNeil recalled more than 130 million bottles of children's medicines like Tylenol, Benadryl, and Motrin because of manufacturing problems at a plant in Fort Washington, Pa. Some of the drugs had the wrong ingredient levels, and others contained tiny particles of metal.

In afternoon trading, Johnson & Johnson shares rose 50 cents to $61.11.

Campbell Soup Supply Company is recalling approximately 15,000,000 pounds of "SpaghettiOs with Meatballs" canned products due to possible under-processing.

The following products are subject to recall:

• 14.75-ounce cans of "SpaghettiOs" with Meatballs, bearing the identifying product code "U5" on the bottom of the can.
• 14.75-ounce cans of "SpaghettiOs" A to Z with Meatballs, bearing the identifying product code "4N" on the bottom of the can.
• 14.75-ounce cans of "SpaghettiOs" Fun Shapes with Meatballs (Cars), bearing the identifying product code "KS" on the bottom of the can.

The products subject to recall bear the establishment number "EST 4K," as well as a "Use By" date between June 2010 and December 2011 ink-jetted on the bottom of each can. These products were manufactured between December 2008 and June 2010 and distributed to retail establishments nationwide. When available, the retail distribution list(s) will be posted on FSIS' website at http://www.fsis.usda.gov/FSIS_Recalls/
Open_Federal_Cases/index.asp.

The problem was discovered through a routine warehouse inspection by the company and its subsequent investigation. FSIS has received no reports of illnesses from consumption of these products.

FSIS routinely conducts recall effectiveness checks to verify recalling firms notify their customers of the recall and that steps are taken to make certain that the product is no longer available to consumers.

Consumer questions regarding the recall should be directed to Campbell's Hotline at (866) 495-3774; media inquiries should be directed to the company's Director of Corporate Communications, Anthony Sanzio at (856) 968-4390.

Marie Callender Recall After Salmonella Outbreak

ConAgra Foods is announcing a precautionary recall of Marie Callender’s Cheesy Chicken & Rice single-serve frozen entrées. Consumers who have this product in their freezer should discard it or return it to their retailer for a refund.

The company has been working closely with state and federal authorities, and while there is no definitive link between the recalled product and any illness, the company is proactively recalling the product after being informed by the U.S. Centers for Disease Control and Prevention of a possible association between the product and eight people in the U.S. who have been diagnosed with salmonellosis linked to Salmonella Chester. CDC interviews have identified individuals who reported eating this product in April and May, 2010. The last reported illness was reported on May 22.

Individuals concerned about an illness should contact a physician. Consumption of food contaminated with Salmonella can cause salmonellosis, a common bacterial food borne illness. Consumers with questions about the recall should contact ConAgra Foods at 1-866-484-9610.

ConAgra Foods produces, markets and sells Marie Callender’s-branded consumer products, all sold in freezer cases at supermarkets and grocery retailers nationwide, under a license agreement with Marie Callender’s Pie Shops, Inc. This recall does not apply to any products sold in Marie Callender’s restaurants.

MCNEIL CONSUMER HEALTHCARE RECALLS FOUR PRODUCT LOTS OF BENADRYL® ALLERGY ULTRATAB™ TABLETS, 100 COUNT, AND ONE PRODUCT LOT OF EXTRA STRENGTH TYLENOL® RAPID RELEASE GELS, 50 COUNT

Fort Washington, PA (June 15, 2010) McNeil Consumer Healthcare, Division of McNEIL-PPC, Inc., is recalling five product lots as an addition to the list of products included in the company’s January 15th, 2010 product recall. The additional lots involved are four product lots of BENADRYL® ALLERGY ULTRATAB™ TABLETS, 100 count, sold in the U.S.; and one product lot of EXTRA STRENGTH TYLENOL® Rapid Release Gels, 50 count sold in the U.S., Trinidad and Tobago, Bermuda, and Puerto Rico (FULL RECALLED PRODUCT LIST BELOW). This recall is a follow-up to the product recall that McNeil Consumer Healthcare announced on January 15th, 2010 and is being taken because the products were inadvertently omitted from the initial recall action. McNeil Consumer Healthcare identified the omission and informed the U.S. Food and Drug Administration (FDA) of its decision to add these product lots to the recall list. All these products were produced before the January 15th, 2010 recall. Since January, McNeil Consumer Healthcare has continued to analyze and evaluate 2,4,6-tribromoanisole (TBA) and has shared that information with the FDA. This further analysis confirms that the risk of serious adverse medical events is remote. This recall is being conducted with the knowledge of the FDA.

BENADRYL® ALLERGY ULTRATAB™ TABLETS is sold over-the-counter and is indicated for the relief of allergy associated symptoms such as sneezing, runny nose, itchy throat, and itchy and watery eyes. EXTRA STRENGTH TYLENOL® Rapid Release Gels is sold over-the-counter and is indicated for the temporary reduction of fever and for the temporary relief of minor aches and pains due to headache, muscular aches, backache, minor arthritis pain, the common cold, toothache, pre-menstrual and menstrual cramps, and flu.

The January 15th, 2010 recall was initiated as a result of consumer complaints of a musty or moldy odor that has since been linked to the presence of trace amounts of a chemical called 2,4,6-tribromoanisole (TBA). After a thorough investigation, it was determined that the source of TBA was the result of a breakdown of a chemical that is applied to wood used to build wooden pallets that transport and store product packaging materials.

Consumers who purchased product from the lots included in this recall should stop using the product and contact McNeil Consumer Healthcare for instructions on a refund or replacement. For these instructions or information regarding how to return or dispose of the product, consumers should log on to the internet at www.mcneilproductrecall.com or call 1-888-222-6036 (Monday-Friday 8 a.m. to 8 p.m. Eastern Time, and Saturday-Sunday 9 a.m. to 5 p.m. Eastern Time). Requests for reimbursement can be made at www.mcneilproductrecall.com. Consumers who have medical concerns or questions should contact their healthcare provider.

Any adverse reactions may also be reported to the FDA’s MedWatch Program by fax at 1-800-FDA-0178, by mail at MedWatch, HF-2, FDA, 5600 Fishers Lane, Rockville, MD 20852-9787, or on the MedWatch website at www.fda.gov/safety/medwatch/default.htm.

Kroger Ice Cream Recalled in Ohio, 16 States

Are you, or is someone you know allergic to tree nuts? Kroger has just recalled Kroger Deluxe Chocolate Paradise Ice Cream because the packaging does not specify that it may contain tree nuts.

This recall does not affect those without nut allergies as there is no other reason for this recall. Those who are allergic may have serious allergic reactions if they consume this product. Kroger is asking consumers who have allergies to return the recalled product(s) to place of purchase for a full refund.

Only very specific Kroger stores and affilates are affected by this recall including Kroger stores in Alabama, Arkansas, Georgia, Illinois, Indiana, Kentucky, Louisiana, Michigan, Mississippi, Missouri, North Carolina, Ohio, South Carolina, Tennessee, Texas, Virginia and West Virginia.

Jay C, Food 4 Less, Hilander, Owen’s, Pay Less and Scott’s stores in Illinois and Indiana are also affected by this recall, but no other Kroger affilaite stores are included.

Kroger Deluxe Chocolate Paradise Ice Cream in 48-ounce containers with a "sell by" date of Jan 24 11 with a UPC Code: 11110 50712 are being recalled.

Consumers who have questions or concerns may contact Kroger at (800) 632-6900.

Dritz™ Electric Scissors Recalled by Prym Due to Fire and Burn Hazards

About 12,000 Dritz Quick Cut™ Electric Scissors, distributed by Prym Consumer USA, of Spartanburg, SC, have been recalled. The electric scissors can overheat, posing fire and burn hazards. Prym Consumer USA has received two reports of the electric scissors igniting causing minor property damage. No injuries have been reported.

The electric scissors are white and blue, about 10" long and include an AC adaptor. "Dritz" is written on the handle on the blue grip. These were sold at Jo-Ann Fabric and Craft Stores and other craft stores nationwide from September 2009 through February 2010 for about $50.

Return the scissors to store where purchased or mail directly to Prym Consumer USA for a refund. If mailing to Prym, please include the product, your complete name, mailing address and phone number in the package and mail to Prym Consumer USA Recall Center, 950 Brisack Road, Spartanburg, SC 29303.

For additional information, contact the firm at 800-255-7796 Monday through Friday 8:00 a.m. to 5:00 p.m. ET, by e-mail at customer.service@prym-consumer-usa.com or on the firm's website at www.prym-consumer-usa.com

GE RECALLS FRONT LOAD WASHING MACHINES

WASHINGTON, D.C. (CPSC) -- The U.S. Consumer Product Safety Commission, in cooperation with the firm named below, today announced a voluntary recall of the following consumer product. Consumers should stop using recalled products immediately unless otherwise instructed. It is illegal to resell or attempt to resell a recalled consumer product.

Name of product: GE Front-Load Washing Machines

Units: About 181,000

Manufacturer: GE Appliances & Lighting, of Louisville, Ky.

Hazard: A wire can break in the machine and make contact with a metal part on the washtub while the machine is operating, posing fire and shock hazards to consumers.

Incidents/Injuries: GE is aware of seven incidents in which flames escaped the units and caused minor smoke damage. No injuries have been reported.

Description: This recall involves GE front-load washing machines without auxiliary water heating. Model and serial numbers are listed below. Recalled washing machines were made between December 2006 and February 2010. The model and serial numbers are located on the bottom right side and on the bottom door frame of the washers.

Brand: GE

Model number begins with: WBVH5

Serial number begins with: AM, AR, AS, AT, DM, DR, DS, FM, FR, FS, GM, GS, HM, HR, HS, LM, LR, LS, MM, MR, MS, RM, RR, RS, SM, SR, SS, TM, TR, TS, VM, VR, VS, ZL, ZM, ZR, ZS

Sold at: Department and various retail stores nationwide from December 2006 through May 2010 for about $700.

Made in: China

Remedy: Consumers should immediately stop using the recalled washers, unplug it from the electrical outlet and contact GE for a free repair. Consumers should not operate the washer until it has been repaired.

Consumer Contact: For more information, contact GE toll-free at 888-345-4124 between 8 a.m. and 5 p.m. ET Monday through Friday, or visit the firm's website at www.geappliances.com.

IKEA RECALLS ROLLER, ROMAN, & ROLL UP BLINDS

WASHINGTON, D.C. (CPSC) -- The U.S. Consumer Product Safety Commission and Health Canada, in cooperation with the firm named below, today announced a voluntary recall of the following product.

Consumers should stop using products immediately unless otherwise instructed. It is illegal to resell or attempt to resell a recalled consumer product.

Name of Product: Roller, Roman, and Roll-Up blinds

Units: About 3,360,000 (About 790,000 Roman blinds were recalled in November 2008 and August 2009 and about 533,000 Roller blinds were recalled in October 2009)
Distributor: IKEA Home Furnishings, of Conshohocken, Pa.

Hazards:

Roller Blinds
Strangulations can occur if the blind’s looped bead chain is not attached to the wall or the floor with the tension device provided and a child’s neck becomes entangled in the free-standing loop.

Roman Blinds
Strangulations can occur when a child places his/her neck between the exposed inner cord and the fabric on the backside of the blind or when a child pulls the cord out and wraps it around his/her neck. An additional hazard exists when the Roman blind has a continuous looped bead chain that if not attached to the wall or floor, which poses a strangulation hazard to children.

Roll-up Blinds
Strangulations can occur if the lifting loops slide off the side of the blind and a child’s neck becomes entangled on the free-standing loop or if a child places his/her neck between the lifting loop and the roll-up blind material.

Incidents/Injuries:

Roman blinds: CPSC and IKEA received a new report of a 1 ½-year old boy in Lowell, Massachusetts who suffered a near strangulation in February 28, 2010. On April 4, 2008, a 1-year-old girl in Greenwich, Conn. became entangled in the inner cord of an IKEA Roman blind and strangled. CPSC and IKEA also received a report of a 2-year old boy who suffered a near strangulation. The last two incidents prompted previous recalls.
Roll-up blinds: No incidents reported.
Roller blinds: No incidents reported.

Description: This recall involves roller blinds that do not have a tension device attached to the bead chain, all Roman blinds and all roll-up blinds.

Sold at: IKEA stores nationwide from January 1998 through June 2009 for between $5 and $55.

Manufactured in : India, Estonia, China, and Poland.

Remedy: Consumers should immediately stop using the roller blinds that do not have a tension device attached to the chain, all Roman blinds and all roll-up blinds and return them to any IKEA store for a full refund. In a previous recall, IKEA reminded consumers who have roller blinds with a tension device attached to the bead chain to make sure the tension device is installed into the wall or floor. If the consumer has difficulty installing the tension device, contact IKEA for additional information.

Consumer Contact : For additional information, contact IKEA toll-free at (888) 966-4532 anytime, or visit the firm’s website at www.ikea-usa.com

Note: Examine all shades and blinds in your home. Make sure there are no accessible cords on the front, side, or back of the product. CPSC recommends the use of cordless window coverings in all homes where children live or visit.

CPSC is still interested in receiving incident or injury reports that are either directly related to this product recall or involve a different hazard with the same product. Please tell us about it by visiting https://www.cpsc.gov/cgibin/incident.aspx.

GM Recalling 1.5M Vehicles Over Fire Concerns

WASHINGTON (AP) -- General Motors Co. said Tuesday it was recalling about 1.5 million vehicles worldwide to address a problem with a heated windshield wiper fluid system that could lead to a fire, its second recall over the issue in two years.

The recall affects several pickup trucks, sport utility vehicles, crossovers and passenger car models from the 2006 to 2009 model years. GM conducted a similar recall in 2008 but came across new reports of fires in vehicles that had been fixed.

GM said it would disable the heated washer fluid system module that could lead to fires. The Detroit automaker will pay owners and those leasing vehicles $100 each since the feature is being disabled.

GM said it was aware of five fires but there had been no injuries or crashes reported. Nearly 1.4 million vehicles are in the U.S. and more than 100,000 vehicles are in Canada, Mexico and other international markets.

"While our analysis shows the number of incidents is very small compared with the number of vehicles on the road, we want our customers to have complete peace of mind," said Jeff Boyer, GM's executive director of safety.

The recall covers the 2006-2009 model year Buick Lucerne, Cadillac DTS, and Hummer H2; 2008-2009 Buick Enclave and Cadillac CTS; 2007-2009 Cadillac Escalade, Escalade ESV and Escalade EXT; 2007-2009 Chevrolet Avalanche, Silverado, Suburban and Tahoe; 2007-2009 GMC Acadia, Sierra, Yukon and Yukon XL; 2007-2009 Saturn Outlook; and 2009 Chevrolet Traverse.

The auto company said customers will begin to receive recall letters later this month but can contact their dealer to make an appointment to have the heated washer system removed. Dealers will remove the heated washer fluid module and reroute washer fluid hoses.

GM said the technology was available from only one supplier, Microheat Inc., of Farmington Hills, Mich., which went out of business, preventing GM from working with another supplier on an improved design.

GM recalled more than 900,000 vehicles because of the heated washer fluid system in August 2008 because a short circuit on the circuit board could overheat the ground wire. The National Highway Traffic Safety Administration had opened an investigation in February 2008 into 2007 Yukon and Tahoe vehicles over potential engine compartment fires.

The government closed its investigation after the 2008 recall but GM later came across fires in vehicles that had been fixed under the previous recall, prompting the latest safety action.

Owners can contact Buick at (866) 608-8080, Cadillac at (866) 982-2339, Chevrolet at (800) 630-2438, Saturn at (800) 972-8876, GMC at (866) 996-9463 and Hummer at (800) 732-5493.