FAF Inc. Recalls Children’s Necklaces From Walmart: Cadmium
January 31, 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.
NAME OF PRODUCT: CHILDREN’S METAL NECKLACES
UNITS: ABOUT 55,000
CFMOTO Powersports Recalls Certain Scooters
January 31, 2010
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Honda Fit Recall – Fire Hazard: 2007-2008 Model Fits
January 30, 2010
Honda is recalling 141,000 Honda Fit vehicles in which a malfunctioning switch can cause the vehicle to overheat and catch fire. This issue may occur when extreme amounts of moisture from rain or melted snow flood the driver’s side master power window switch.
NHTSA Press Release on the Toyota Floor Mat Recall
January 30, 2010
Also see:
Toyota Recall: Four Different Causes. So Which is it?
Toyota Corolla and Toyota Scion Recall Brake Issues
Toyota Recalls 3.8 Million Vehicles: Gas Pedals Sticking
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Budget Rental Car Company Issues Statement About Recalled Toyotas
January 29, 2010
Also see: Toyota Recall: Four Different Causes. So Which is it?
The following email was sent to Budget rental car company customers today:
Yesterday Budget announced that it was removing all of the vehicles identified for recall by Toyota from its corporate fleet in the US, Canada, and Puerto Rico. This step was taken to protect the safety of our customers, which is always our top priority.
Recalled Infusion Set Needles Manufactured by Nipro for Exelint
January 29, 2010
Recall Classification: Class I
Date Recall Initiated: December 23, 2009
Product Names:
* Exel Huber Needles
* EXELint Huber Needles
* Exel Huber Infusion Sets
* EXELint Huber Infusion Sets
* Exel “Securetouch+” Huber Safety Sets
* EXELint Huber Safety Sets
ALL LOT NUMBERS BEGINNING WITH 07, 08, OR 09 ARE AFFECTED BY THIS RECALL.
Hettich Centrifuges with 2050 and 2076 Plastic Rotors
January 29, 2010
FDA notified healthcare professionals of a Class I recall of Hettich Centrifuges with 2050 and 2076 plastic rotors, used in combination with the Mikro 12-24, Mikro 20, Haematokrit 20 and Haematokrit 24 bench top plastic centrifuges. The recall was initiated because the plastic centrifuge rotor may crack, break apart and be forcefully ejected through the plastic centrifuge housing at a high rate of speed. This may result in serious personal injury and damage to the surrounding area.
Edwards Lifesciences Aquarius Hemodialysis System
January 29, 2010
FDA and Edwards Lifesciences notified healthcare professionals of a Class I recall of the Aquarius Hemodialysis System due to reports of clinically significant fluid imbalance and the potential for users to repeatedly override the fluid imbalance alarm. This could result in a decrease or increase in the volume of the circulating blood, which may result in serious injuries or death.
Starbucks Recalls Glass Water Bottles Due to Cut Hazard
January 29, 2010
WASHINGTON, DC – 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 PRODUCTS. CONSUMERS SHOULD STOP USING RECALLED PRODUCTS IMMEDIATELY UNLESS OTHERWISE INSTRUCTED.
NAME OF PRODUCT: GLASS WATER BOTTLES
Summit Treestands Recalls Hunting Tree Stand Brackets Due to Fall Hazard
January 29, 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.
NAME OF PRODUCT: TALON HUNTING HANG-ON TREE STANDS AND BRACKETS/STRAPS
FDA Recalls Exel/Exelint Huber Needles
January 28, 2010
FDA Announces Class I Recall of Certain Infusion Set Needles
Huber needles used in implanted ports to withdraw blood, inject medications, and other solutions
The U.S. Food and Drug Administration today announced a Class I recall of Exel/Exelint Huber needles, Exel/Exelint Huber Infusion Sets and Exel/Exelint “Securetouch+” Safety Huber Infusion Sets, manufactured by Nipro Medical Corporation for Exelint International Corporation.
Liebherr RecallsRefrigerators Due to Injury Hazard
January 28, 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 PRODUCTS. CONSUMERS SHOULD STOP USING RECALLED PRODUCTS IMMEDIATELY UNLESS OTHERWISE INSTRUCTED.
NAME OF PRODUCT: LIEBHERR BUILT-IN 24-INCH WIDE SINGLE DOOR REFRIGERATORS
UNITS: ABOUT 2,700
CYBEX Strollers Recalled: Risk of Fingertip Amputation
January 28, 2010
WASHINGTON, DC – 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 PRODUCTS. CONSUMERS SHOULD STOP USING RECALLED PRODUCTS IMMEDIATELY UNLESS OTHERWISE INSTRUCTED.
NAME OF PRODUCT: CYBEX STROLLERS
Yamaha Recalls Snowmobiles: Loss of Steering Control
January 28, 2010
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.
NAME OF PRODUCT: 2009 MODEL YEAR FX10 SNOWMOBILES
UNITS: ABOUT 2,500
DISTRIBUTOR: YAMAHA MOTOR CORPORATION U.S.A., OF CYPRESS, CALIF.
Zippo Recalls Candle Lighters Due to Burn Hazard
January 28, 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 PRODUCTS. CONSUMERS SHOULD STOP USING RECALLED PRODUCTS IMMEDIATELY UNLESS OTHERWISE INSTRUCTED.
NAME OF PRODUCT: ZIPPO SLATKIN & CO. CANDLE LIGHTERS
UNITS: ABOUT 17,500
Well Luck Co. Recalls Instant Noodles From China
January 28, 2010
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Winnebago Recalls Certain Motor Homes: Crash Risk
January 28, 2010
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Vectra And Itasca Recalls Motor Homes
January 28, 2010
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Kawasaki Recalls Certain Motorcycles: Crash Risk
January 28, 2010
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Holiday Rambler Recalls Certain RVs: Crash Risk
January 28, 2010
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