Jaguar Recalls Certain 2010-2011 Jaguar XK Vehicles

July 25, 2010

Vehicle Make / Model:     Model Year(s):
     JAGUAR / XF     2010
     JAGUAR / XK     2010-2011
Manufacturer: JAGUAR LAND ROVER NORTH AMERICA, LLC Mfr’s Report Date: JUL 21, 2010
NHTSA CAMPAIGN ID Number: 10V332000 N/A NHTSA Action Number: N/A

Nissan Recalls Certain 2009-2010 Nissan Cube Cars

July 25, 2010

Vehicle Make / Model:     Model Year(s):
     NISSAN / CUBE     2009-2010
Manufacturer: NISSAN NORTH AMERICA, INC. Mfr’s Report Date: JUL 21, 2010
NHTSA CAMPAIGN ID Number: 10V330000 N/A NHTSA Action Number: N/A
Component: FUEL SYSTEM, GASOLINE:STORAGE

CPSC Announces Pool and Spa Kids Safety Education Effort

July 24, 2010

HUNDREDS OF POOL AND SPA INCIDENTS SINCE MEMORIAL DAY WEEKEND

HOUSTON – HALFWAY THROUGH THE SUMMER SWIMMING SEASON, THE U.S. CONSUMER PRODUCT SAFETY COMMISSION (CPSC) HAS SEEN NEWS REPORTS OF MORE THAN 210 CHILD DROWNING AND NON-FATAL SUBMERSION INCIDENTS IN POOLS AND SPAS AROUND THE COUNTRY SINCE MEMORIAL DAY WEEKEND. IN AN EFFORT TO REDUCE THESE PREVENTABLE INCIDENTS, CPSC AND PARTNERS SAFE KIDS USA AND THE NATIONAL DROWNING PREVENTION ALLIANCE (NDPA) JOINED FORCES TODAY TO INTRODUCE A NEW KIDS SAFETY EDUCATION PROGRAM. THE CENTERPIECES OF THE PROGRAM ARE A MULTI-PART EDUCATIONAL VIDEO AND AN ONLINE ACTIVITY, WHICH ARE PART OF CPSC’S NATIONAL POOL SAFELY CAMPAIGN.

J & H Besta Corp. Recalls Joyful Slim Herb Supplement Found to Contain an Undeclared Drug

July 23, 2010

J & H Besta Corp. of Hicksville, NY, has been informed by the Food and Drug Administration (FDA) that FDA lab analysis of Joyful Slim Herb Supplement distributed by the company was found to contain undeclared Desmethyl 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.

DeBoles Nutritional Foods Recalls One Lot Code of DeBoles Kids Only! Gluten Free Tubettini Corn Pasta: Undeclared Allergen

July 23, 2010

DeBoles Nutritional Foods, Inc. announced that it is recalling one lot code of DeBoles® Kids Only! Gluten Free Tubettini Corn Pasta because it may contain undeclared whole wheat alphabet pasta. People who are allergic to wheat run the risk of an allergic reaction, which may be serious or life-threatening if they consume the recalled product.

Near Strangulation Prompts Recall of Roman and Roller Shades by Smith+Noble

July 23, 2010

SMITH+NOBLE HAS ADDED ITS NAME TO THE RETAILERS JOINING THE VOLUNTARY RECALL ANNOUNCED IN DECEMBER 2009 OF ALL ROMAN SHADES AND ROLL-UP BLINDS.

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.

Cook Recalls Certain Ciaglia Blue Rhino and Ciaglia Blue Dolphin Percutaneous Tracheostomy Introducer Sets and Trays

July 22, 2010

Cook has initiated a voluntary recall of certain lots of its Ciaglia Blue Rhino and Ciaglia Blue Dolphin Percutaneous Tracheostomy Introducer Sets and Trays that contain a Covidien 6PERC or 8PERC Shiley™ Tracheostomy Tube.

Atico International USA Recalls Bamboo Torches Due to Laceration Hazard

July 22, 2010

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.

Good Health, Inc. Recalls Vialipro – Contains Prescription-Only Ingredients

July 21, 2010

Good Health, Inc. announced today that it is conducting a voluntary nationwide recall of the company’s dietary supplement Vialipro for sexual enhancement sold under the Lot Numbers listed below.

Pacifiers Recalled by Antonio Flores Due to Choking Hazard

July 21, 2010

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.

Georgia Firm Recalls Frozen Chicken Nugget Products That May Contain Foreign Materials

July 20, 2010

Recall Release CLASS II RECALL
FSIS-RC-046-2010 HEALTH RISK: LOW

Congressional and Public Affairs
(202) 720-9113
Adrian Gianforti

WASHINGTON, July 19, 2010 – Perdue Farms, Inc., a Perry, Ga. establishment, is recalling approximately 91,872 pounds of frozen chicken nugget products that may contain foreign materials, the U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) announced today.

D & M Smoked Fish, Inc. Issues an Allert on Uneviscerated Schmaltz Herring

July 18, 2010

D & M Smoked Fish, Inc. located in Queens, New York, is recalling Haifa brand vacuum packaged Schmaltz Herring with the lot number 168, because the product was found to be uneviscerated.

J & H Besta Corp. Recalls Slim- 30 Herb Supplement Found to Contain an Undeclared Drug Ingredient

July 18, 2010

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.

Fresh Express Recalls Expired Romaine Lettuce with Use-By Dates of July 8 to 12 and S in the Product Code

July 16, 2010

Fresh Express is voluntarily recalling certain Romaine lettuce salad products with expired Use-by Dates of July 8 – 12 and an S in the Product Code because they may have the potential to be contaminated with E. coli O157:H7. No other Fresh Express salads are included in the recall.

Feline’s Pride Expands Recall of Natural Chicken Formula Cat Food: Salmonella Contamination

July 16, 2010

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.

Child’s Death Prompts Recall to Repair Portable Playard Tent by Tots in Mind

July 16, 2010

WASHINGTON, D.C. – THE U.S. CONSUMER PRODUCT SAFETY COMMISSION (CPSC) AND HEALTH CANADA (HC), IN COOPERATION WITH TOTS IN MIND INC., OF SALEM, N.H., IS ANNOUNCING THE VOLUNTARY RECALL TODAY OF ABOUT 20,000 (AND 85 IN CANADA) COZY INDOOR OUTDOOR PORTABLE PLAYARD TENTS PLUS CABANA KITS.

Baja Motorsports Recalls Mini Bikes and Go-Carts Due to Fire and Burn Hazards

July 16, 2010

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.

Bristol-Myers Squibb Recalls Coumadin (R) 1 mg Tablet Blister Packs

July 15, 2010

Bristol-Myers Squibb is recalling three lots of physician sample blister packs of Coumadin® 1 mg tablets and five lots, of Coumadin 1 mg tablet hospital unit dose (HUD) blister packs.

QFC Recalls Broccoli Raisin Salad for Undeclared Allergen

July 15, 2010

Quality Food Center (QFC) stores said today it is recalling select containers of Broccoli Raisin Salad because they may contain walnuts not listed on the label.

Customers should return the product to stores for a full refund or replacement.

Diamond Usa Inc. Issues Allergy Alert On Undeclared Sulfites In Dry Apricot Rolled

July 15, 2010

Diamond USA Inc. is recalling its 1 lb packages with code#01-12-2010 of “Dry Apricot Rolled” because they contain undeclared sulfites. People who have severe sensitivities to sulfites run the risk of serious or life-threatening allergic reaction if they consume this product.

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