Pointe Scientific Recalls Liquid Glucose Hexokinase Reagent (G7517)
October 31, 2009
Pointe Scientific, Inc, Canton, MI is initiating a nationwide recall of all size kits of Liquid Glucose Hexokinase Reagent catalog number G7517. The reagents have been found to fail linearity at >200mg/dL that results in inaccurate glucose values above this range.
Cordis Recalls Crpsspver Sheath Introducer
October 31, 2009
Cordis Corporation announced today a nationwide voluntary recall of all lots of the CROSSOVER™ Sheath Introducer due to complaints about stretching or fracture of the sheath during use.
Mazda Truck Recall – Fire Risk
October 31, 2009
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Mrs. Rios Corn Products Issues Allergy Alert on Undeclared Whey in Flour Tortillas
October 30, 2009
Mrs. Rios Corn Products in San Angelo, Texas is recalling its flour tortillas because they may contain undeclared Whey. People who have an allergy or severe sensitivity to Whey run the risk of serious or life-threatening allergic reaction if they consume these products.
Chinese Drywall Studies Released by CPSC, EPA, HUD, CDC, and ATSDR
October 30, 2009
The US Consumer Product Safety Commission (CPSC) has received thousands of reports involving corroding metal components in houses built using Chinese drywall materials. The Chinese Drywall complaints and reports come from 30 US States, the District of Columbia and Puerto Rico.
CPSC Warns About Burn and Laceration Hazards this Halloween
October 30, 2009
SOON THE GHOULS AND GOBLINS OF HALLOWEEN NIGHT WILL PROWL NEIGHBORHOOD STREETS IN SEARCH OF TREATS. THE U.S. CONSUMER PRODUCT SAFETY COMMISSION (CPSC) WANTS TO ENSURE THAT CANDLE FLAMES FROM JACK-O-LANTERNS, DECORATIVE OBSTACLES ON THE PORCH OR LAWN, AND SHARP EDGES ON COSTUMES AND ACCESSORIES DON’T KEEP KIDS FROM ENJOYING THIS ANNUAL TRADITION OF TRICK-OR-TREATING.
Popas Bakery Inc. Issues Allergy on Undeclared Whey (Milk) in all Flour Tortillas
October 29, 2009
Popas Bakery Inc. Issues Allergy on Undeclared Whey (Milk) in all Flour Tortillas
Halloween Flashlights Sold Exclusively at Target Recalled Due to Burn Hazard
October 29, 2009
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: HALLOWEEN FLASHLIGHTS
UNITS: ABOUT 610,000
Sony Recalls Computer AC Adapters Due to Shock Hazard
October 29, 2009
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: SONY VAIO COMPUTER AC ADAPTERS
UNITS: ABOUT 69,000
Iowa Firm Pinnacle Foods Recalls Chili With Beans Product
October 29, 2009
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Mia Moda Infant Child Restraints – Car Seats
October 29, 2009
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Orion Transit Buses ( 09V413000 )
October 29, 2009
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San Link Inc. Issues an Alert on Uneviscerated Vacuum Pack Dried Krasnoperka (Fish).
October 28, 2009
San Link Inc. Issues an Alert on Uneviscerated Vacuum Pack Dried Lesh (Fish).
October 28, 2009
San Link Inc at 54B Marjorie Street Staten Island, NY 10309 is recalling Vacuum Pack Dried Lesh (fish) because the product was found to be uneviscerated.
The recalled Vacuum Pack dried Lesh (fish) was distributed in New York State, New Jersey State and Connecticut State in vacuum pack containers. The Vacuum Pack Dried Lesh (fish) is a product of Russia.
Qualitest Pharmaceuticals Issues a Voluntary Nationwide Recall of All Accusure® Insulin Syringes
October 28, 2009
Huntsville AL-Qualitest Pharmaceuticals today issued a voluntary nationwide recall of all Accusure Insulin Syringes. The distributed syringes are of the following descriptions and NDC numbers: 28G 1/2cc, NDC 0603-6995-21;28G 1cc, NDC 0603-6996-21; 29G 1/2cc NDC 0603-6997-21, 29G 1cc, NDC 0603-6998-21, 30G 1/2cc, NDC 0603-999-21, 30G 1cc, NDC 0603-7000-21, 31G 1/2cc, NDC 0603-7001-21; and 31G 1cc, NDC 0603-7002-21. All Accusure® Insulin Syringes regardless of lot number are subject to this recall. These syringes were distributed between January 2002 and October 2009 to wholesale and retail pharmacies nationwide (including Puerto Rico). The syringes in these lots may have needles which detach from the syringe.
Belkin International Inc. Recalls SurgeMaster Surge Protectors Due to Shock Hazard
October 28, 2009
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: SURGEMASTER™ SURGE PROTECTORS
UNITS: ABOUT 68,700
Risk of Strangulation Prompts Recall to Repair IKEA Roller Blinds
October 28, 2009
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: ISDANS, TUPPLUR, AND ENJE ROLLER BLINDS
UNITS: ABOUT 533,000
Near Strangulation of Child Prompts Recall of Roman Shades by Whole Space; Sold Exclusively by Hanover Direct/Domestications
October 28, 2009
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: FAUX SUEDE ROMAN SHADES
UNITS: ABOUT 90,000
Near Strangulation of Children Prompts Recall of Roman Shades by Louis Hornick & Co
October 28, 2009
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: DUBLIN ENERGY SOLUTION ROMAN SHADES
UNITS: ABOUT 364,000
Mars Snackfood US ISSUES ALLERGY ALERT ON UNDECLARED PEANUTS In Dove Caramel Pecan Perfection Ice Cream
October 27, 2009
Mars Snackfood US announced a voluntary recall of its Dove Caramel Pecan Perfection ice cream with the lot number 931AB5YN07 because it may contain undeclared peanuts. People who have an allergy or severe sensitivity to peanuts run the risk of serious or life-threatening allergic reaction if they consume these products. No related illnesses have been reported to date. For consumers who do not suffer from a peanut allergy or sensitivity, this product is safe to eat. The lot number is found on the bottom of the containers.
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