Hawaii247.com | Hawaii 24/7

MEDIA RELEASE

The Hartz Mountain Corporation Recalls Hartz Naturals Real Beef Treats Because of Possible Salmonella Health Risk

The Hartz Mountain Corporation is voluntarily recalling one specific lot of Hartz Naturals Real Beef Treats for Dogs due to concerns that one or more bags within the lot may have been potentially contaminated with Salmonella. Hartz is fully cooperating with the US Food and Drug Administration in this voluntary recall.

Salmonella is an organism which can cause serious infections in young children, frail or elderly people, and others with weakened immune systems, all of whom are at particular risk from exposure and should avoid handling these products.

Salmonella symptoms may include fever, diarrhea, abdominal pain, and nausea in both dogs and humans. Anyone experiencing the symptoms of Salmonella infection should seek immediate medical attention. Owners of dogs exhibiting these symptoms should also seek veterinary assistance.

Hartz Mountain Corporation is recalling 74,700 8-oz bags of Hartz Naturals Real Beef Treats for Dogs, lot code BZ0969101E, UPC number 32700-11519, which were imported by Hartz from a Brazilian supplier, Bertin S.A., and which were distributed to a number of customers in the United States. While regular testing conducted by Bertin (prior to shipment to the US) did not detect the presence of Salmonella in any packages of this product, random sample testing conducted by FDA did indicate the presence of Salmonella. Hartz is aggressively investigating the source of the problem.

Although Hartz has not received any reports of animals or humans becoming ill as a result of coming into contact with this product, Hartz is taking immediate steps to remove the product from all retail stores and distribution centers. Dog owners having purchased this product should check the lot code on their bag, and, if the code is not visible, or if the bag has lot code BZ0969101E imprinted thereon, they should immediately discontinue use of the product and discard it in a proper manner.

Consumers can contact Hartz at 1-800-275-1414 at any time with any questions they may have and for information on how to obtain reimbursement for purchased product.

MEDIA RELEASE

WASHINGTON, D.C. – 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 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: Satellite T135, Satellite T135D and Satellite ProT130 Notebook Computers

Units: About 41,000 worldwide

Manufacturer: Toshiba America Information Systems Inc., of Irvine, Calif.

Hazard: The notebook computers can overheat at the notebook’s plug-in to the AC adapter, posing a burn hazard to consumers.

Incidents/Injuries: Toshiba has received 129 reports of the notebook computers overheating and deforming the plastic casing area around the AC adapter plug, including two reports of minor burn injuries that did not require medical attention and two reports of minor property damage.

Description: This recall involves certain Toshiba Satellite T135, Satellite T135D and Satellite Pro T130 notebook computer models. “Toshiba” is printed on the top of the notebook computer. The model name and number are printed on a label on the bottom of the notebook computers.

Sold at: Electronics stores and other retailers nationwide and online, including at Toshibadirect.com and other websites, from August 2009 through August 2010 for between $600 and $800.

Manufactured in: China

Remedy: Consumers should immediately download the latest version of Toshiba’s BIOS computer program to their notebook computer at http://laptops.toshiba.com/about/consumer-notices. This new computer program will detect whether the notebook computer is overheating, and if so, disable the notebook computer’s external power and display a message directing the consumer to contact Toshiba for a free repair. Consumers who do not have Internet access should contact Toshiba to arrange for installation of the updated BIOS.

Consumer Contact: For additional information, contact Toshiba at (800) 457-7777 anytime or visit the firm’s website at http://laptops.toshiba.com/about/consumer-notices

Note: Health Canada’s press release is available at http://cpsr-rspc.hc-sc.gc.ca/PR-RP/recall-retrait-eng.jsp?re_id=1157

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

MEDIA RELEASE

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

Regulator with a "G"

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

MEDIA RELEASE

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 online retailers, including www.albeebaby.com and 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

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

MEDIA RELEASE

Glow Industries, Inc., Perrysburg, OH, announced today that it is initiating a voluntary nationwide recall of the company’s product sold under the name of Mr. Magic Male Enhancer from Don Wands. Glow Industries, Inc. is conducting this voluntary recall after being informed by the Food and Drug Administration (FDA) that lab analysis has found the Mr. Magic Male Enhancer from Don Wands capsules to contain Hydroxythiohomosildenafil and Sulfoaildenafil, an analogue of Sildenafil, an FDA-approved drug used in the treatment of male Erectile Dysfunction (ED), making Mr. Magic Male Enhancer an unapproved new drug. These active ingredients are not listed on the product label. Product manufactured containing lot numbers 9041401, 251209 and 8121904 are included in this recall.

The Mr. Magic Male Enhancer recall includes:

The recall is being conducted as a precautionary measure. No illnesses or adverse effects have been reported to the company to date in connection with the product.

The undeclared ingredients may pose a threat to consumers because the analogue may interact with nitrates found in some prescription drugs (such as nitroglycerin) and may lower blood pressure to dangerous levels. Consumers with diabetes, high blood pressure, high cholesterol, or heart disease often take nitrates. ED is a common problem in men with conditions, and consumers may seek types of products to enhance sexual performance.

Glow Industries, Inc. advises any customer in possession of Mr. Magic Male Enhancer from Don Wands capsules to call (419) 350-2726, between the hours of 8 a.m and 5 p.m, Monday through Friday, Eastern Standard Time for instructions on the product return and credit process. Glow Industries, Inc. is notifying its distributors and retailers by a recall letter and phone calls to arrange for return of recalled product in their possession.

Any adverse events that may be related to the use of this product should be reported to the FDA’s MedWatch Adverse Event Reporting program online [at www.fda.gov/MedWatch/report.htm], by returning the postage-paid FDA form 3500 [which may be downloaded from www.fda.gov/MedWatch/getforms.htm] by mail [to MedWatch, 5600 Fishers Lane, Rockville, MD 20852-9787] or fax [1-800-FDA-0178].

Customers with questions should contact Glow Industries, Inc. at (419) 350-2726.

MEDIA RELEASE

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

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

MEDIA RELEASE

The following product safety recall was voluntarily conducted by the firm in cooperation with the CPSC. 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: 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

—

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

MEDIA RELEASE

The following product safety recall was voluntarily conducted by the firm in cooperation with the CPSC. 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: Kawasaki 2010 KLX110 Off-Road Motorcycles

Units: About 4,000

Distributors: Kawasaki Motors Corp. U.S.A., of Irvine, Calif.

Hazard: A faulty housing for the ignition switch can allow water to enter and activate the electric starter unintentionally. This poses a serious hazard of injury or death.

Incidents/Injuries: No injuries have been reported.

Description: This recall involves Kawasaki 2010 model year KLX110CAF and KLX110DAF off-road motorcycles. They were sold in green and have Kawasaki written on the sides of the fuel tank.

Sold by: Kawasaki dealers nationwide from August 2009 through February 2010 for about $2,100.

Manufactured in: Thailand

Remedy: Consumers should stop using these vehicles immediately and contact a local Kawasaki Motorcycle dealer to schedule an appointment for a free repair. The company has attempted to contact all known users.

Consumer Contact: For more information, consumers can contact Kawasaki toll-free at (866) 802-9381 between 8:30 a.m. and 5 p.m. PT Monday through Friday, or visit the firm’s website at www.kawasaki.com

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

MEDIA RELEASE

J & H Besta Corp. Issues a Voluntary Nationwide Recall of Slim- 30 Herb Supplement Found to Contain an Undeclared Drug Ingredient

J & H Besta Corp. of Hicksville, NY, has been informed by the Food and Drug Administration (FDA) that FDA lab analysis of Slim-30 Herb Supplement distributed by the company was found to contain undeclared N-Desmethyl Sibutramine and traces of Sibutramine. Sibutramine is an FDA-approved drug used as an appetite suppressant for weight loss. The FDA has not approved this product, therefore the safety and effectiveness of the product is unknown.

FDA advises that this product poses a threat to consumers because Sibutramine is known to substantially increase blood pressure and/or pulse rate in some patients and may present a significant risk for patients with a history of coronary artery disease, congestive heart failure, arrhythmias or stroke.

Slim-30 Herb Supplement is marketed as a Natural Herb for Weight Loss. Slim-30 Herb Supplement is packaged in plastic bottles containing 30 capsules per bottle and bears UPC 8 31457 005009 2. The affected lot/code being recalled is 032009. The product was sold to distributors and retail stores nationwide and China and via internet sales.

No illnesses or injuries have been reported to the company to date in connection with this product.

J & H Besta Corp. is taking this voluntary action because of the concern for the health and safety of consumers. The company has discontinued distribution of this affected product lot. It sincerely regrets any inconvenience to our customers.

Consumers should not consume the Slim-30 Herb Supplement and should return it immediately to the place of purchase for a full refund. Consumers with questions should contact Jason Wang at 516-735-1436, Monday through Friday, 10:00 am to 5:30 pm, EDT.

Any adverse reactions experienced with the use of this product may be reported to the FDA’s MedWatch Safety Information and Adverse Event Reporting Program online [at www.fda.gov/MedWatch/report.htm9], by phone 1-800-332-1088 [1-800-FDA-1088], or by returning the postage-paid FDA form 3500 [which may be downloaded from the MedWatch "Download Forms10" page], by mail [to address on the pre-addressed form] or fax [1-800-FDA-0178].

This recall is being conducted with the knowledge of the U.S. Food and Drug Administration.

Feline’s Pride Expands Nationwide Recall of its Natural Chicken Formula Cat Food Due to Salmonella Contamination

MEDIA RELEASE

Feline’s Pride is expanding its July 1, 2010 voluntary recall of Feline’s Pride Raw food with ground bone for cats and kittens, Natural Chicken Formula, Net Wt. 2.5 lbs. (1.13 kg., 40 oz.) produced on 6/10/10 to include the product produced on 6/21/10, because it may be contaminated with Salmonella. People handling raw pet food can become infected with Salmonella, especially if they have not thoroughly washed their hands after having contact with the raw pet food or any surfaces exposed to the product.

When consumed by humans, Salmonella can cause an infection, salmonellosis. The symptoms of salmonellosis include nausea, vomiting, abdominal cramps, minimal diarrhea, fever, and headache. Certain vulnerable populations, such as children, the elderly, and individuals with compromised immune systems, are particularly susceptible to acquiring salmonellosis from such pet food products and may experience more severe symptoms.

Pets with Salmonella infections may be lethargic and have diarrhea or bloody diarrhea, fever, and vomiting. Some pets will have only decreased appetite, fever and abdominal pain. 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.

The product is packaged in uncoded plastic containers and sold frozen to private consumers nationwide. Once thawed, the pet food has a shelf life of about 1 week. The firm manufactures the pet food by an as-ordered basis. This expansion of the recall affects those orders placed and shipped from June 21 through June 26, 2010 (produced on 6/21/10).

The firm and FDA are investigating this matter to determine the source of this problem, and will take any additional steps necessary to protect the public health.

To date, both the firm and the FDA have received no reports of Salmonella infection relating to this product.

People who are experiencing the symptoms of Salmonella infection after having handled the pet food product should seek medical attention, and report their use of the product and illness to the nearest FDA office.

People should thoroughly wash their hands after handling the pet food – especially those made from raw animal protein such as meat or fish — to help prevent infection. People may risk bacterial infection not only by handling pet foods, but by contact with pets or surfaces exposed to these foods, so it is important that they thoroughly wash their hands with hot water and soap.

Since certain vulnerable populations, such as children, the elderly, and individuals with compromised immune systems, are particularly at risk from exposure they should avoid handling this product.

Consumers with questions should contact the company at (716) 580-3096, Monday -Friday from 10 am – 4 pm EDT.

MEDIA RELEASE

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: 2010 Redline Conquest Cyclocross Bicycles and Framesets

Units: About 330

Distributor: Seattle Bike Supply, of Kent, Wash.

Hazard: The bicycle fork’s legs can separate from the fork crown and cause the rider to lose control, posing a fall hazard and risk of injury.

Incidents/Injuries: The firm has received five reports of cracks near the fork’s crown.

Description: This recall involves all 2010 Redline Conquest Cyclocross bicycles and framesets. The bicycles and framesets were sold in yellow and black, and have aluminum frames and aluminum forks with aluminum steering tubes. “Redline” is printed on the bicycle frame. The bicycles are equipped with a 700C wheel and frame sizes ranging from 44cm to 60 cm.

Sold at: Bicycle specialty stores nationwide between July 2009 through May 2010 for about $1,400 for the bicycle and $400 for the frameset.

Manufactured in: Taiwan

Remedy: Consumers should immediately stop using the recalled bicycles and framesets and contact their local Redline bicycle dealer to receive a free fork replacement.

Consumer Contact: For additional information, contact Redline Bicyles at (800) 283-2453 between 9:00 a.m. and 5:00 p.m. PT Monday through Friday, or visit the firm’s website at www.redlinebicycles.com

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

MEDIA RELEASE

The following product safety recall was voluntarily conducted by the firm in cooperation with the CPSC. 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: Television Sets

Units: About 2,700

Importer/Distributor: PDi Communications Inc., of Springboro, Ohio

Hazard: A capacitor on the television’s power supply board can fail, posing a fire hazard.

Incidents/Injuries: PDi Communications has received one report of an incident involving a flame in February 2010. No injuries have been reported.

Description: This recall involves 26-inch and 32-inch wall-mounted LCD television sets that were installed in healthcare facilities, such as hospitals, medical centers and nursing homes. Model and serial number ranges included in this recall are listed in the chart below. The model number is printed on a label on the back of the television sets. Other models of PDi television sets or units that are outside the serial number range are not included in this recall.

Sold by: PDi Communications to distributors that service healthcare facilities such as hospitals, medical centers and nursing homes nationwide from September 2008 through July 2009 for about $1,000.

Manufactured in: China

Remedy: Immediately stop using the recalled television sets, remove the power cord to prevent the TV from being powered on and contact PDi to receive a free repair. PDi began contacting healthcare facilities about this problem in March. Facilities that have not been contacted by PDi or its authorized agent should contact the firm for a free repair.

Consumer Contact: For more information, contact PDi at (800) 992-7734 between 8 a.m. and 4:30 p.m. ET Monday through Friday, or visit the firm’s website at www.pdiarm.com