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 … [Read more...]
Archives for November 2009
COUNTRY COACH ( 09V439000 )
Vehicle Make / Model: Model Year(s): COUNTRY COACH / RHASPODY 2007-2008 Manufacturer: COUNTRY COACH INC Mfr's Report Date: NOV 09, 2009 NHTSA CAMPAIGN ID Number: 09V439000 N/A NHTSA Action Number: N/A Component: ENGINE AND ENGINE COOLING Potential Number of … [Read more...]
Recalled Maclaren Baby Strollers
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. Every Maclaren folding "umbrella" stroller sold in the United States since 1999 is being recalled, … [Read more...]
Hospira Recalls Certain Lots of Liposyna and Propofol Products: May Contain Particulate Matter
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 … [Read more...]
Edwards Lifesciences CardioVations EndoClamp Aortic Catheter
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. Use: The device blocks off the aorta, monitors aortic pressure, … [Read more...]
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