Timpte Recalls Certain Trailers: Injury Risk

October 31, 2010

Vehicle Make / Model:     Model Year(s):
     TIMPTE / TDH     2009-2011
Manufacturer: TIMPTE, INC. Mfr’s Report Date: OCT 15, 2010
NHTSA CAMPAIGN ID Number: 10V515000 N/A NHTSA Action Number: N/A
Component: EQUIPMENT:MECHANICAL
Potential Number of Units Affected: 279

BMW Recalls Certain 08 X5 SAVs With 6-Cylinder Engines

October 31, 2010

Vehicle Make / Model:     Model Year(s):
     BMW / X5     2008
Manufacturer: BMW OF NORTH AMERICA, LLC Mfr’s Report Date: OCT 26, 2010
NHTSA CAMPAIGN ID Number: 10V518000 N/A NHTSA Action Number: N/A
Component: FUEL SYSTEM, GASOLINE:DELIVERY:FUEL PUMP

Keystone Recalls Certain RVs: Fire Hazard

October 31, 2010

Vehicle Make / Model:     Model Year(s):
     KEYSTONE / EVEREST     2003-2004
     KEYSTONE / MONTANA     2001-2005
     KEYSTONE / MONTANA-BIG SKY     2001-2005
Manufacturer: KEYSTONE RV COMPANY Mfr’s Report Date: OCT 26, 2010

Open Range Recalls Certain RVs: Refriderator

October 31, 2010

Vehicle Make / Model:     Model Year(s):
     OPEN RANGE / OPEN RANGE     2011
     OPEN RANGE / RESIDENTIAL     2011
     OPEN RANGE / ROLLING THUNDER     2011
Manufacturer: OPEN RANGE R.V. COMPANY Mfr’s Report Date: OCT 22, 2010

Damon RVs with Atwood Ovens Recalled

October 31, 2010

Vehicle Make / Model:     Model Year(s):
     DAMON / DAYBREAK     2011
     FOUR WINDS INTERNATIONAL / FREEDOM ELITE     2011
     FOUR WINDS INTERNATIONAL / HURRICANE     2011
Manufacturer: THOR INDUSTRIES Mfr’s Report Date: OCT 26, 2010

Four Winds International Recalls Certain RVs with Atwood Ovens

October 31, 2010

Vehicle Make / Model:     Model Year(s):
     DAMON / DAYBREAK     2011
     FOUR WINDS INTERNATIONAL / FREEDOM ELITE     2011
     FOUR WINDS INTERNATIONAL / HURRICANE     2011
Manufacturer: THOR INDUSTRIES Mfr’s Report Date: OCT 26, 2010

B. Braun Recalls Heparin: Contaminant

October 30, 2010

B. Braun Medical Inc. (B. Braun) was recently notified by its supplier, Scientific Protein Laboratories LLC (SPL), of a nationwide recall of a lot of Heparin Sodium USP Active Pharmaceutical Ingredient (API) sold to B. Braun because additional testing of retained crude heparin samples used by SPL to manufacture this single API lot indicated a trace amount of oversulfated chondroitin sulfate (OSCS) contaminant. As a result, B. Braun is initiating a voluntary recall of seven lots of heparin injection products to the healthcare provider level. These lots were manufactured in 2008 and will be expiring on October 31, 2010 and November 30, 2010.

Kosher First Recalls Tuv Taam Salads Nova Lox Salad: Listeria

October 30, 2010

KOSHER FIRST LLC. 502 FLUSHING AVE. is recalling TUV TAAM SALADS NOVA LOX SALAD due to Listeria monocytogenes contamination.

Listeria monocytogenes is an organism which can cause serious and sometimes fatal infections in young children, frail, or elderly people and others with weakened immune systems. Although healthy persons may suffer only short-term symptoms such as high fever, severe headache, stiffness, nausea, abdominal pain and diarrhea, Listeria infection can cause miscarriages and stillbirths among pregnant women.

The Children’s Place Recalls Girls’ Ruffle Vests: Choking Hazard

October 30, 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. IT IS ILLEGAL TO RESELL OR ATTEMPT TO RESELL A RECALLED CONSUMER PRODUCT.

NAME OF PRODUCT: WHITE RUFFLE OUTDOOR VESTS

UNITS: APPROXIMATELY 3,300

Nissan Recalls Certain Models: Crash Risk

October 30, 2010

Vehicle Make / Model:     Model Year(s):
     INFINITI / QX56     2004-2006
     NISSAN / ARMADA     2004-2006
     NISSAN / FRONTIER     2005-2006
     NISSAN / PATHFINDER     2005-2006
     NISSAN / TITAN     2004-2006

INFINITI ( 10V517000 )

October 30, 2010

Vehicle Make / Model:     Model Year(s):
     INFINITI / QX56     2004-2006
     NISSAN / ARMADA     2004-2006
     NISSAN / FRONTIER     2005-2006
     NISSAN / PATHFINDER     2005-2006
     NISSAN / TITAN     2004-2006

Ford Recalls Certain Edge and Lincoln: Electronic Locks

October 30, 2010

Vehicle Make / Model:     Model Year(s):
     FORD / EDGE     2011
     LINCOLN / MKX     2011
Manufacturer: FORD MOTOR COMPANY Mfr’s Report Date: OCT 25, 2010
NHTSA CAMPAIGN ID Number: 10V516000 N/A NHTSA Action Number: N/A

Lincoln Recalls Certain Models: Electronic Locks

October 30, 2010

Vehicle Make / Model:     Model Year(s):
     FORD / EDGE     2011
     LINCOLN / MKX     2011
Manufacturer: FORD MOTOR COMPANY Mfr’s Report Date: OCT 25, 2010
NHTSA CAMPAIGN ID Number: 10V516000 N/A NHTSA Action Number: N/A

Suzuki Recalls Certain Models: Loose Mirrors

October 30, 2010

Vehicle Make / Model:     Model Year(s):
     SUZUKI / SX4     2007-2010
Manufacturer: AMERICAN SUZUKI MOTOR CORP. Mfr’s Report Date: OCT 18, 2010
NHTSA CAMPAIGN ID Number: 10V513000 N/A NHTSA Action Number: N/A
Component: VISIBILITY:REARVIEW MIRRORS/DEVICES:EXTERIOR

Mitsubishi Recalls Certain: Air Conditioning

October 30, 2010

Vehicle Make / Model:     Model Year(s):
     MITSUBISHI / ENDEAVOR     2006-2008
Manufacturer: MITSUBISHI MOTORS NORTH AMERICA, INC. Mfr’s Report Date: OCT 20, 2010
NHTSA CAMPAIGN ID Number: 10V514000 N/A NHTSA Action Number: N/A
Component: ELECTRICAL SYSTEM: SOFTWARE

Sandoz initiates voluntary recall in the US of all 50mg/2mL and 250mg/10mL vials of Methotrexate Injection, USP due to the presence of glass particulates

October 29, 2010

Sandoz Inc. announced today it has initiated a voluntary recall in the US of all 50mg/2mL and 250mg/10mL vials of Sandoz and Parenta brand Methotrexate Injection, USP product (“methotrexate”) to the consumer/user level. Consistent with its commitment to quality and patient safety, Sandoz is initiating this voluntary recall of all 24 lots of the affected product following the finding of small glass flakes by Sandoz quality control in a limited number of vials in four lots. The flakes are the result of delamination of the glass used to manufacture the vials of these two dosage presentations.

Dollar Tree Recalls Children’s Halloween Lanterns Due to Fire and Burn Hazards

October 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. IT IS ILLEGAL TO RESELL OR ATTEMPT TO RESELL A RECALLED CONSUMER PRODUCT.

CPSC Prevent Halloween Costume and Decoration-Related Injuries

October 29, 2010

WASHINGTON, D.C. – THE U.S. CONSUMER PRODUCT SAFETY COMMISSION (CPSC) WANTS PARENTS OF TRICK-OR-TREATERS TO KNOW THAT THERE IS NOTHING SCARY ABOUT PREVENTING HALLOWEEN-RELATED INJURIES. BY TAKING A FEW SIMPLE SAFETY PRECAUTIONS WHEN SELECTING COSTUMES AND HALLOWEEN DECORATIONS, CONSUMERS CAN PREVENT BURN, FALL AND LACERATION INJURIES.

Bicycles Recalled by Easton Sports: Fall Hazard

October 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. IT IS ILLEGAL TO RESELL OR ATTEMPT TO RESELL A RECALLED CONSUMER PRODUCT.

bioMerieux, Inc. Issues Urgent Product Correction for VITEK 2 Gram Negative Susceptibility Cards Containing Piperacillin/Tazobactam

October 28, 2010

bioMerieux, Inc. on September 16, 2010, initiated a worldwide voluntary product correction of VITEK ® 2 Gram Negative Susceptibility Cards containing the antibiotic Piperacillin/Tazobactam (TZPv). These cards, manufactured after March 10, 2009, are used in clinical laboratories to perform antimicrobial susceptibility testing as part of the VITEK® System. Clinical laboratories were notified to perform an alternative method of testing prior to reporting results for:

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