Archives for 2009

LIFEPAK CR Plus Automated External Defibrillators

September 17, 2009 By The FDA Leave a Comment

FDA notified healthcare professionals of a Class I recall of certain LIFEPAK CR Plus Automated External Defibrillators (AED) manufactured and distributed from July 9, 2008 through August 19, 2008. An extremely humid environment may cause the affected devices to improperly analyze the heart rhythm and may cause the device to delay or fail to deliver … [Read more...]

Garlic Press/Slicers Recalled by Trudeau Corporation

September 17, 2009 By The CPSC Leave a Comment

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: TRUDEAU GARLIC DUO SLICERS UNITS: ABOUT 22,000 MANUFACTURER: TRUDEAU … [Read more...]