FOR IMMEDIATE RELEASE
November 5, 2009
Release # 10-032 Firm’s Recall Hotline: (866) 319-5335
CPSC Recall Hotline: (800) 638-2772
CPSC Media Contact: (301) 504-7908
Children’s Art Easels Recalled by MacPherson’s Due to Violation of Lead Paint Standard

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.

Name of Product: Young Artist Easels

Units: About 10,000

Manufacturer: MacPherson’s, of Emeryville, Calif.

Hazard: The chalkboard surface coating contains high levels of lead, violating the federal lead paint standard.

Incidents/Injuries: None reported.

Description: This recall involves a children’s art easel which has a chalkboard surface on one side and a white board surface on the other side. The item number is AA13301 and the UPC number is 082435133010 which can be found on the original packaging.

Sold at: Art supply stores nationwide and online from July 2004 through June 2009 for about $75.

Manufactured in: China

Remedy: Consumer should immediately take these recalled easels away from children and contact the firm to receive a free replacement chalkboard panel.

Consumer Contact: For additional information, contact MacPherson’s at (866) 319-5335 between 8 a.m. and 4:30 p.m. PT Monday through Friday, visit the firm’s Web site at www.art-alternatives.com/recall or send email to recall@macphersonart.com

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.

Name of Product: Gehl’s HOT TOP2 Nacho Cheese and Chili Sauce Dispensers

Units: About 115,000

Manufacturer: Gehl Foods Inc., of Germantown, Wis.

Hazard: The dispenser’s fan blade can come into contact with the heater coil, posing fire and burn hazards to consumers.

Incidents/Injuries: Gehl Foods has received 12 reports of the dispenser’s fan blade malfunctioning and coming into contact with the heater coil, including one report of a fire that caused property damage. No injuries have been reported.

Description: This recall includes Gehl Food’s commercial nacho cheese and chili sauce dispensers with model numbers HT2-04 Single, HT2-04 Dual, and HT2-03 APS with serial numbers HT2 164500 through HT2 299689. The model and serial numbers are located on the back of the dispensers. “Gehl’s” is printed on the front of the dispensers.

Sold at: The dispensers were leased to commercial customers nationwide, including concession and food service establishments, from December 2003 through September 2009.

Manufactured in: United States

Remedy: Food establishments and consumers should immediately stop using the recalled nacho cheese and chili sauce dispensers and contact the firm for a free repair by Gehl, or to receive a free repair kit to be installed by the customer.

Consumer Contact: For more information, contact Gehl Foods toll-free at (877) 440-4008 between 8 a.m. and 4:30 p.m. CT Monday through Friday or visit the firms’ Web site at www.gehls.com

Media Inquiries: Rita Chappelle, 301-796-4672, rita.chappelle@fda.hhs.gov
Consumer Inquiries: 888-INFO-FDA

FDA Health Alert for Certain Pet Treats Made by Pet Carousel
Products may be contaminated with Salmonella
The U.S. Food and Drug Administration is issuing this health alert to warn consumers not to use Pig Ears and Beef Hooves pet treats manufactured by Pet Carousel because the products may be contaminated with Salmonella. The products were distributed nationwide in both bulk and retail packaging for sale in pet food and retail chain stores. Pet Carousel is based in Sanger, Calif.

The products were manufactured under conditions that facilitate cross-contamination within batches or lots. Although no illnesses associated with these products have been reported, the FDA is advising consumers in possession of these products to not handle or feed them to their pets.

The affected pig ear products were packaged under the brand names Doggie Delight and Pet Carousel. The affected beef hooves were packaged under the brand names Choo Hooves, Dentley’s, Doggie Delight, and Pet Carousel. All sizes and all lots of these products made by Pet Carousel are included in this alert.

During September 2009, the FDA conducted routine testing of pig ears made by Pet Carousel. The test results detected a positive reading for Salmonella. This prompted an FDA inspection of Pet Carousel’s manufacturing facilities. During the inspection, the agency collected additional pet treat samples. Further analysis found Salmonella present in beef hooves, pig ears and in the manufacturing environment.

Salmonella can affect both humans and animals. People handling dry pet food and/or pet treats can become infected with Salmonella, especially if they have not thoroughly washed their hands after having contact with the treats or any surfaces exposed to these products. Consumers should dispose of these products in a safe manner by securing them in a covered trash receptacle.

Healthy people infected with Salmonella may experience some or all of the following symptoms: nausea, vomiting, diarrhea or bloody diarrhea, abdominal cramping and fever. Although rare, Salmonella can result in more serious ailments including arterial infections, endocarditis (inflammation of the lining of the heart), arthritis, muscle pain, eye irritation, and urinary tract symptoms. Consumers exhibiting these signs after having contact with this product should contact their health care provider immediately.

Pets with Salmonella infections may become lethargic and have diarrhea or bloody diarrhea, fever and vomiting. Some pets may only experience a 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 any of the affected products or is experiencing any of these symptoms, contact your veterinarian immediately.

FOR IMMEDIATE RELEASE — Phoenix, AZ, Nov 4, 2009 - PetSmart (NASDAQ: PETM) is voluntarily recalling two Dentley’s Beef Hoof products for potential salmonella contamination. The products were manufactured by Pet Carousel, Inc. in Sanger, Calif.

The recalled products include only the following types of Dentley’s Beef Hooves purchased between Oct. 2, 2009 and Nov. 3, 2009:

Dentley’s Bulk Cattle Hoof UPC# 73725703323
Dentley’s 10 Pack Beef Hooves UPC# 73725736055

No other products are included in this recall.

The affected products were shipped from the Pet Carousel plant to three PetSmart distribution centers in Ottawa, Ill.; Groveport, Ohio and Newnan, Ga.; and then shipped directly to certain PetSmart stores. Although the affected product was not shipped to every store, as a precautionary measure PetSmart immediately recalled the product from all of its US stores and instituted a register block to prevent any product from being inadvertently scanned and sold. In addition, PetSmart removed the product from the PetSmart.com Web site and notified PetPerks customers with valid e-mail addresses in the PetSmart database who purchased the affected products.

Salmonellosis is an infection with bacteria called salmonella. Most persons infected with salmonella develop diarrhea, fever, and abdominal cramps 12 to 72 hours after infection. The illness usually lasts four to seven days, and most persons recover without treatment. However, in some individuals, the diarrhea may be so severe that the patient needs to be hospitalized. In these patients, the salmonella infection may spread from the intestines to the blood stream, and then to other body sites and can cause death unless the person is treated promptly with antibiotics. The elderly, infants, and those with impaired immune systems are more likely to have a severe illness.

Many dogs do not show clinical signs of salmonella. However, when they do, they often have diarrhea or other signs of systemic infections.

Customers who purchased the recalled products should discontinue use immediately and return the product to any PetSmart store for a complete refund or exchange. Customers who have concerns about their health or their pet’s health should consult a medical professional. For additional information about the recall, customers can visit www.petsmartfacts.com, www.petsmart.com ; www.fda.govor contact PetSmart Customer Service at 1-888-839-9638.

PetSmart, Inc. is the largest specialty pet retailer of services and solutions for the lifetime needs of pets. The company operates more than 1,145 pet stores in the United States and Canada, 156 in-store PetSmart PetsHotel(R) cat and dog boarding facilities, and is a leading online provider of pet supplies and pet care information (www.petsmart.com). PetSmart provides a broad range of competitively priced pet food and pet products; and offers complete pet training, pet grooming, pet boarding, Doggie Day Camp(SM) pet day care services and pet adoption services. Since 1994, PetSmart Charities, Inc., an independent 501(c)(3) non-profit animal welfare organization, has funded more than $87 million in grants and programs benefiting animal welfare organizations and, through its in-store pet adoption programs, has helped save the lives of more than 3.7 million pets.

FOR MORE INFORMATION:
www.petsmartfacts.com
customercare@petsmart.com
1-888-839-9638

NEWS MEDIA CONTACT:
Jessica White
PetSmart Media Line (623) 587-2177
mediarelations@ssg.petsmart.com

SOURCE: PetSmart, Inc.
http://www.petsmartfacts.com
mailto:customercare@petsmart.com
mailto:mediarelations@ssg.petsmart.com

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Company Contact:
Judith Moore
843-762-4186

FOR IMMEDIATE RELEASE – November 3, 2009 – Charleston Cookie Company of Charleston, SC is recalling packages of Almond Cookies which were sold as a component of the Dean and Deluca “Americana” cookie tin because the cookies contain undeclared butter (milk).

People who have allergies to milk products run the risk of serious or life-threatening allergic reaction if they consume these products.

The recalled Almond Cookies were distributed to Dean & Deluca for resale as part of their “Americana Cookie” collection. The product comes in a 6 ounce, clear plastic package sold with 5 other flavors of cookies in a 36 oz. silver tin. The product bears no code or UPC but was distributed to Dean & Deluca in August 2009 for sale in their catalog and online.

No illnesses have been reported to date in connection with this problem.

The recall was initiated after it was discovered that the milk-containing product was distributed in packaging that did not indicate the presence of butter (milk). Investigation indicates that the problem was caused by a temporary breakdown in the company’s packaging process. The situation has been rectified by production of a new label with a complete ingredients listing.

Consumers who have purchased the product are urged to return them to the place of purchase for a full refund. Consumers with questions may contact Charleston Cookie Company at 843-762-4186. Business hours are Monday through Friday from 8 am to 5 pm.

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Company Contact:
Walter Tozzi, R.Ph., M.S., M.B.A.
Director of Marketing and Professional Services
631-924-4000

FOR IMMEDIATE RELEASE - November 3, 2009 - Shirley, NY - American Regent conducts nationwide voluntary recall of ALL lots of its Ketorolac Tromethamine Injection, USP 15 mg/mL:

NDC# 0517-0601-25 15 mg/mL 1mL Single Dose Vial

PLEASE NOTE: This recall is in addition to the voluntary recall initiated on October 16, 2009 when American Regent voluntarily recalled ALL unexpired lots of Ketorolac Tromethamine Injection, USP, 30 mg/mL due to the presence of particulate matter in conjunction with crystallization.

This voluntary recall is due to the potential that particulates from crystallization may be present in the product. American Regent is undertaking this recall in consideration of the potential for safety issues if the product is administered to patients, including obstruction of blood vessels which can induce pulmonary emboli or thrombosis, activate platelets and/or neutrophils to induce anaphylactic reactions. Other adverse effects associated with the injection of particulate matter include foreign body granulomas, and local irritation at the injection site.

The product was distributed to wholesalers and distributors nationwide.

Hospitals, surgi-centers, clinics and other healthcare facilities should not use any AMERICAN REGENT Ketorolac Tromethamine Injection, USP Injection 15 mg/mL for patient care and should immediately quarantine any product for return.

“Patient safety is our primary concern, and we are committed to taking the necessary steps to protect patients from any potential safety risks as we continue to investigate this issue” said Mary Jane Helenek, President and CEO of American Regent.

While American Regent continues to investigate this issue, the company is taking precautionary action and initiated this voluntary recall. American Regent has informed the FDA of its actions and is maintaining ongoing discussions with the Agency.

As is standard practice, and as stated in the Ketorolac Tromethamine Injection Product Package Insert, “Parenteral drug products should be inspected visually for particulate matter and discoloration prior to administration whenever solution and container permit”

American Regent will credit accounts for all returned Ketorolac Tromethamine Injection, USP product. Those with questions about the return process, please call our Customer Service Department at 1-800-645-1706: Monday thru Friday from 8:30 AM to 7:00 PM ET.

Hospitals, surgi-centers, clinics and healthcare providers, or patients with other questions may contact the Professional Services Department at 631-924-4000.

Any adverse reactions experienced with the use of this product, and/or quality problems should be reported to American Regent, Inc. via email at PV@luitpold.com, by fax to 610-650-7781 or 610-650-0170 or by phone at 1-800-734-9236. Adverse reactions may also be reported to FDA’s MedWatch Adverse Event Reporting program online, or by returning the postage paid FDA form 3500, by mail to [MedWatch, 5600 Fishers Lane, Rockville, MD 20852-9787] or via fax [1-800-FDA-0178].

Ketorolac Tromethamine Injection, USP is manufactured by Luitpold Pharmaceuticals, Inc. and is distributed by American Regent, Inc. (Shirley, NY).

Company Contact:
Mary O’Donnell,
727-733-8399

FOR IMMEDIATE RELEASE - November 3, 2009 - Dunedin, Fl – Pelican Bay Ltd. of Dunedin, Florida is recalling all their Caramel Chocolate Truffle Hot Chocolate Mix because it may contain undeclared tree nuts. People who have an allergy or severe sensitivity to tree nuts run the risk of serious or life-threatening allergic reaction if they consume these products.

Caramel Chocolate Truffle Hot Chocolate Mix was distributed domestically through direct delivery, mail order and through retail stores. This product is also shipped to Canada, United Kingdom, Japan and the Netherlands. Product distributed between January 2007 and November 2, 2009 is subject to this recall.

Caramel Chocolate Truffle Hot Chocolate Mix is packaged in a cone shape poly bag with a hanging tag attached to the front of the package and SKU# 3204, UPC 94522 01015 on the back of the label.

No illnesses have been reported to date.

The recall was initiated after it was discovered that product containing tree nuts was distributed in packaging that did not reveal the presence of tree nuts.

Consumers who have purchased Caramel Chocolate Truffle Hot Cocoa Mix manufactured by Pelican Bay LTD are urged to call 1-800-826-8982, 9AM to 5 PM EST for information on product returns and replacement.

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Company Contact:
1-866-236-8417
service@bodybuilding.com

FOR IMMEDIATE RELEASE - Boise, ID - November 3, 2009 – As part of its ongoing cooperation with the Food and Drug Administration (”FDA”), Bodybuilding.com, LLC (the “Company”) announced today that it is conducting a voluntary nationwide and international recall of all lots and expiration dates of 65 dietary supplement products (the “Recalled Products”) described on the attached list, that were sold through the Company’s website, www.bodybuilding.com.

The FDA has informed the Company that it believes that the Recalled Products contain ingredients that are steroids. Specifically, the FDA has advised the Company of its concern that the Recalled Products may contain the following ingredients that are currently classified, or the FDA believes should be classified, as steroids: “Superdrol,” “Madol,” “Tren,” “Androstenedione,” and/or “Turinabol.” While the Company has not had an opportunity to independently confirm the FDA’s concerns that the Recalled Products in fact contain these ingredients, the Company is undertaking this voluntary recall in an abundance of caution.

Acute liver injury is known to be a possible harmful effect of using steroid-containing products. In addition, steroids may cause other serious long-term adverse health consequences in men, women, and children. These include shrinkage of the testes and male infertility, masculinization of women, breast enlargement in males, short stature in children, a higher predilection to misuse other drugs and alcohol, adverse effects on blood lipid levels, and increased risk of heart attack, stroke, and death.

The Company has not received to date any reports of adverse events in connection with the Recalled Products. Because of the possible harmful effects of using products containing steroids, the Company is cooperating with the FDA to conduct a recall of the products the FDA has identified as containing steroids. Prior to agreeing to carry the Recalled Products, the Company received assurances from all of the manufacturers of the Recalled Products that these products were properly classified as dietary supplements in compliance with federal law, meaning that these products did not contain any unlawful ingredient. Customers who have any of the Recalled Products in their possession should stop using them immediately and contact their physician if they have experienced any problems that may be related to taking one or more of the ingredients listed above.

Any adverse events that may be related to the use of the Recalled Products should be reported to the FDA’s MedWatch Adverse Event Reporting program online [at www.fda.gov/MedWatch/report.htm], by phone [1-800-FDA-1088], or by returning the postagepaid 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].

The Company is committed to providing accurate information about its products. The Company is working voluntarily with the FDA in this recall process.

Consumers should return any unused products purchased on the Company’s site to the Company. For instructions on how to return Recalled Products please call (1-866-236-8417) or e-mail (service@bodybuilding.com) the Company.

RECALLED PRODUCT LIST

Brand Name
4Ever Fit D-Drol

Advanced Muscle Science Dienedrone

Advanced Muscle Science Liquidrone UTT

Anabolic Xtreme Hyperdrol X2

APS (aka Advanced Muscle Science) Mastavol

APS (aka Advanced Muscle Science) Revamp

APS (aka Advanced Muscle Science) Ultra Mass Stack

APS (aka Advanced Muscle Science) Ripped Stack

Better Body Sports Finadex

Black China Labs Straight Drol

Black China Labs Straight Phlexed

Body Conditioning Solutions TestraFLEX

Bjorklund Methyldrostanolone

BOSC Enterprises Epi-Tren

BOSC Enterprises Magna Drol

Chaparral Labs Epivol

Chaparral Labs Pheravol-V

Competitive Edge Labs M-Drol

Competitive Edge Labs P-Plex

Competitive Edge Labs X-tren

Diabolic Labs Epio-Plex

Diabolic Labs Finabolic 50

Diabolic Labs Revenge

Ergopharm 6-OXO

Ergopharm 6-OXO Extreme

EST (aka Engineered Sports Technology) MethAnstance

Extreme Labs Susto-Test Depot

Fizogen ON Cycle II Hardcore

G.E.T/ (Genetic Edge Technologies) SUS-500

G.E.T/ (Genetic Edge Technologies) Tren-250

Hardcore Formulations T-Roid

I Force Nutrition 1,4 AD Bold 200

I Force Dymethazine/Reversitol Combo Pack

I Force Reversitol

I Force Nutrition 17a PheraFLEX

I Force Nutrition Dymethazine

I Force Nutrition Methadrol

IDS (aka Innovative Delivery Systems) Bromodrol

IDS (aka Innovative Delivery Systems) Grow Tabs TR

IDS (aka Innovative Delivery Systems) Mass Tabs

IDS (aka Innovative Delivery Systems) Oxodrol Pro

IDS (aka Innovative Delivery Systems) Ripped Tabs TR

IDS (aka Innovative Delivery Systems) Rapid Release

Ripped Tabs

Kilo Sports Massdrol

Kilo Sports Phera-Mass

Kilo Sports Trenadrol

Monster Caps Monster Caps

Myogenix Spawn

Nutra Coastal D-Stianozol

Nutra Coastal H-Drol

Nutra Coastal MDIT

Nutra Coastal S-Drol

Nutra Coastal Trena

Performance Anabolics Methastadrol

Performance Anabolics Tri-Methyl X

Purus Labs E-pol Inslinsified

Purus Labs Nasty Mass

Rage RV2

Rage RV3

Rage RV4

Rage RV5

Redefine Nutrition Finaflex 550-XD

Redefine Nutrition Finaflex Ripped

Transform Supplements Forged Extreme Mass

Transform Supplements Forged Lean Mass

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Company Contact:
Marti DeMoss
(Office) 208-424-5459 (Cell) 208-908-3549

FOR IMMEDIATE RELEASE – October 30, 2009 – Today, Alexia Foods, Inc, Kennewick, WA, in cooperation with the U.S. Food and Drug Administration (FDA) is voluntarily recalling packages of its Alexia – Olive Oil, Sun-Dried Tomatoes & Pesto Oven Reds (frozen seasoned potato wedges) for an undeclared allergen, pine nuts. People who have an allergy or severe sensitivity to pine nuts run the risk of serious or life-threatening allergic reaction if they consume these products.

The product was distributed to retail stores nationwide.

The affected product, Alexia – Olive Oil, Sun-Dried Tomatoes & Pesto Oven Reds, is packaged in 15 oz. white poly bags with a teal-colored graphic banner and pictures seasoned potato wedges on the front bag panel. This voluntary recall is limited to only packages of Alexia – Olive Oil, Sun-Dried Tomatoes & Pesto Oven Reds bearing the following Sell By dates (shown below) printed on the upper left back panel of the poly package with the UPC # 34183 00108. No other Alexia frozen or shelf stable products are affected.

Sell By 5385050811 Sell By 5385050911
Sell By 5385051011 Sell By 5385051111

The product was produced with packaging that does not declare pine nuts in the product. Alexia Foods has taken the precautionary measure of notifying the U.S. Food and Drug Administration (FDA) and is voluntarily recalling about 9,000 cases of the product.

Alexia Foods will work with retail customers to ensure that the recalled products are removed from store shelves. In the event that consumers believe they have purchased products affected by this voluntary recall, they should return the product to the store where it was purchased for a full refund. Consumers with questions may call 1-866-518-0894 or visit www.alexiafoods.com for more information.

Alexia Foods is also issuing an alert through the Food Allergy & Anaphylaxis Network (FAAN) in an effort to notify any potentially affected consumers.

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