Roadtrek Motorhome Recall
November 14, 2009
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Jeep Wrangler Recalls: 2007-2008
November 14, 2009
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Mitsubishi Lancer Recall
November 14, 2009
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Synthes USA, Ti Synex II Vertebral Body Replacement
November 13, 2009
| Recall Class: | Class I | ||
| Date Recall
Initiated: |
September 14, 2009 | ||
| Product: |
Ti Synex II Vertebral Body Replacement (VBR)
This recall involves part numbers 04.808.001-11, Synex II Central Body, Titanium (all lots).
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Rechargeable Batteries Used with Touch Panels for Audio/Visual Systems Recalled by AMX Due to Fire and Burn Hazards
November 13, 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: RECHARGEABLE BATTERIES SOLD WITH MVP 5000 SERIES WIRELESS TOUCH PANELS
Treestands Recalled by Gander Mountain Company
November 13, 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: HANG-ON FIXED POSITION TREESTANDS
UNITS: ABOUT 13,000
Backpack Blowers Recalled by Homelite Due to Fire Hazard
November 13, 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: HOMELITE BACKPACK BLOWERS
UNITS: ABOUT 85,000
Bicycles Recalled by Easton Sports: Stem Failure Poses Fall Hazard
November 13, 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: BICYCLES WITH EA30 STEMS
UNITS: ABOUT 6,400
Maclaren USA Recalls to Repair Strollers Following Fingertip Amputations
November 11, 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: MACLAREN STROLLERS
UNITS: ABOUT ONE MILLION
Power Adapters Used with IBM RDX Back Up Disk Hard Drives Recalled Due to Shock Hazard
November 11, 2009
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: POWER ADAPTERS WITH IBM RDX BACK UP HARD DISK DRIVES
UNITS: ABOUT 90
DISTRIBUTOR: IBM, OF RESEARCH TRIANGLE PARK, N.C.
Gehl Foods Recalls Nacho Cheese and Chili Sauce Dispensers: Fire Hazard
November 11, 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: GEHL’S HOT TOP2 NACHO CHEESE AND CHILI SAUCE DISPENSERS
COUNTRY COACH ( 09V439000 )
November 11, 2009
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Recalled Maclaren Baby Strollers
November 10, 2009
Over one-million baby strollers are being recalled in the United States by the British baby stroller brand Maclaren after a dozen children suffered finger amputations as a result of getting fingers stuck in the hinges of these recalled strollers.
Hospira Recalls Certain Lots of Liposyna and Propofol Products: May Contain Particulate Matter
November 10, 2009
Hospira, Inc. (NYSE: HSP), a global specialty pharmaceutical and medication delivery company, is voluntarily recalling 85 lots of Liposynâ?¢ II 10%, Liposyn II 20%, Liposyn III 10%, Liposyn III 20%, Liposyn III 30% and 73 lots of Propofol Injectable Emulsion 1% products that begin with the lot numbers 79 and 80 because some of the containers may contain particulate matter. The source of the particulate matter has been identified as stainless steel equipment used in the manufacturing process. The affected lots were distributed between July 2009 and October 2009, and no other lots are affected by this recall.
Edwards Lifesciences CardioVations EndoClamp Aortic Catheter
November 10, 2009
| Recall Class: | Class I |
| Date Recall
Initiated: |
September 24, 2009 |
| Product: |
CardioVations EndoClamp Aortic Catheter, Model Numbers EC1001 and EC65 This product was manufactured from August, 2008 through August, 2009 and distributed from November, 2008 through September, 2009. |
Maclaren USA Recalls to Repair Strollers Following Fingertip Amputations
November 10, 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: MACLAREN STROLLERS
UNITS: ABOUT ONE MILLION
Pointe Scientific Liquid Glucose Hexokinase Reagent – Recall
November 7, 2009
Pointe Scientific and FDA notified healthcare professionals of 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. Distributors and testing laboratories who have received the Liquid Glucose Hexokinase Reagent (G7517) which is being recalled should destroy remaining inventory.
Jelly Belly Issues Allergy Alert on Undeclared Peanuts in 7.5oz cylinder-style packages of 49 Flavors Jelly Belly jelly beans
November 7, 2009
Jelly Belly Candy Company is recalling 7.5-ounce cylinder-style packages of 49 Flavors Jelly Belly jelly beans because the package is incorrectly labeled. The mislabeled packages failed to list peanut butter and peanut flour in the ingredient statement. People who have an allergy to peanuts or a severe sensitivity to peanuts run the risk of serious or life-threatening allergic reaction if they consume these ingredients.
DODGE ( 09V418000 )
November 7, 2009
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PetSmart Recalls Dentley’s Beef Hooves
November 6, 2009
PetSmart is 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
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