Penumbra and FDA notified healthcare professionals about a voluntary field removal of the original version of Neuron 6F 070 Delivery Catheter due to reports that the catheter could kink or ovalize in certain anatomical situations, lead to difficulty in catheter advancement and/or delivery of other devices through the guide catheter. Continued usage … [Read more...]
Triumph Sprint ST 1050 Motorcycle Recall
Vehicle Make / Model: Model Year(s): TRIUMPH / SPRINT ST 1050 2005-2009 Manufacturer: TRIUMPH MOTORCYCLES AMERICA LTD Mfr's Report Date: SEP 29, 2009 NHTSA CAMPAIGN ID Number: 09V378000 N/A NHTSA Action Number: N/A Component: SUSPENSION Potential Number of … [Read more...]
DIAMOND COACH ( 09V373000 )
Vehicle Make / Model: Model Year(s): DIAMOND COACH / VIP 2008-2009 Manufacturer: DIAMOND COACH CORPORATION Mfr's Report Date: SEP 28, 2009 NHTSA CAMPAIGN ID Number: 09V373000 N/A NHTSA Action Number: N/A Component: EQUIPMENT:ELECTRICAL:AIR CONDITIONER … [Read more...]
Additional Injuries Prompt DeVilbiss to Reannounce Recall of Pressure Washers and Air Compressors Due to Fracture and Laceration Hazards
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: DEVILBISS AIR POWER COMPANY PRESSURE WASHERS AND AIR COMPRESSORS … [Read more...]
Guardian Full-Face Diving Masks Recalled by Ocean Technology Due to Visor Separation Hazard
WASHINGTON, D.C. - 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: GUARDIAN FULL-FACE MASKS UNITS: ABOUT 900 MANUFACTURER: … [Read more...]
Wooden Toys Recalled by Daiso Due to Choking Hazard
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: WOODEN TOYS UNITS: ABOUT 430 IMPORTER: DAISO CALIFORNIA LLC, OF … [Read more...]
Daiso Recalls Children's Toys, Purses and Pen Cases Due to Violation of Lead Paint and Phthalate Limits
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 TOYS, PURSES AND PEN CASES UNITS: ABOUT 130 IMPORTER: … [Read more...]
Directors Chairs Sold at Lowe's Recalled Due to Fall Hazard
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: FOLDING DIRECTORS CHAIRS UNITS: ABOUT 84,000 IMPORTER: L G SOURCING INC., OF … [Read more...]
Niles, Ill. Firm Issues Allergy Alert on Classic Candy
Affy Tapple, LLC, a Niles, Ill. firm, is voluntarily recalling its "Limited Edition – Classic Candy Flavors" two-pack caramel apples because the label did not include the allergen statement "manufactured on shared equipment with peanuts and tree nuts". Consumers who have an allergy to peanuts may run the risk of a serious allergic reaction if they … [Read more...]
Decreased Sex Drive in Men: Is Your Low Libido Just Normal?
A decreased sex drive (libido) in men is often a symptom of conditions like low testosterone related to aging, but could also be side effects associated with certain medications. Below is a list of diseases and conditions associated with symptoms like decreased sex drive, as well as a list of medications related to similar side effects. We are not … [Read more...]
Panther Motorcycle Recall – Brake Systems
Vehicle Make / Model: Model Year(s): PANTHER / P150 2008-2009 PANTHER / P50 2008-2009 Manufacturer: PANTHER MOTORS INC Mfr's Report Date: SEP 23, 2009 NHTSA CAMPAIGN ID Number: 09V379000 N/A NHTSA Action Number: N/A … [Read more...]
FREIGHTLINER ( 09V376000 )
Vehicle Make / Model: Model Year(s): FREIGHTLINER / CASCADIA 2008-2009 Manufacturer: DAIMLER TRUCKS NORTH AMERICA Mfr's Report Date: SEP 21, 2009 NHTSA CAMPAIGN ID Number: 09V376000 N/A NHTSA Action Number: N/A Component: AIR BAGS Potential Number of Units … [Read more...]
Recalled Audi A3, TT, TT Roadsters: Fuel Leak: 2006-2010
Vehicle Make / Model: Model Year(s): AUDI / A3 2006-2010 AUDI / TT 2008-2010 AUDI / TT ROADSTER 2008-2010 Manufacturer: VOLKSWAGEN OF AMERICA, INC Mfr's Report Date: SEP 30, … [Read more...]
Philips Recalls Select Heartstart Fr2+ Automated External Defibrillators
Philips is voluntarily recalling approximately 5,400 HeartStart FR2+ automated external defibrillators (AEDs). This recall is being conducted due to the possibility of a memory chip failure that may render the device inoperable. Only certain HeartStart FR2+ AEDs (models M3860A and M3861A, distributed by Philips; and models M3840A and M3841A, … [Read more...]
NABI – North American Bus Industries Recall
Vehicle Make / Model: Model Year(s): NABI / 40LFW 2009 NABI / 45CLFW 2008-2009 Manufacturer: NORTH AMERICAN BUS INDUSTRIES, INC. Mfr's Report Date: SEP 28, 2009 NHTSA CAMPAIGN ID Number: 09V371000 N/A NHTSA Action … [Read more...]
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