WINNEBAGO ( 10V248000 )

June 10, 2010

Vehicle Make / Model:     Model Year(s):
     ITASCA / NAVION     2010
     ITASCA / NAVION IQ     2010
     WINNEBAGO / VIEW     2010
     WINNEBAGO / VIEW PROFILE     2010
Manufacturer: WINNEBAGO INDUSTRIES, INC. Mfr’s Report Date: JUN 01, 2010

ITASCA ( 10V248000 )

June 10, 2010

Vehicle Make / Model:     Model Year(s):
     ITASCA / NAVION     2010
     ITASCA / NAVION IQ     2010
     WINNEBAGO / VIEW     2010
     WINNEBAGO / VIEW PROFILE     2010
Manufacturer: WINNEBAGO INDUSTRIES, INC. Mfr’s Report Date: JUN 01, 2010

SPARTAN ( 10V245000 )

June 10, 2010

Vehicle Make / Model:     Model Year(s):
     SPARTAN / GLADIATOR     2008-2010
     SPARTAN / METROSTAR     2009-2010
Manufacturer: SPARTAN CHASSIS, INC. Mfr’s Report Date: JUN 03, 2010
NHTSA CAMPAIGN ID Number: 10V245000 N/A NHTSA Action Number: N/A

DUTCHMEN ( 10V244000 )

June 10, 2010

Vehicle Make / Model:     Model Year(s):
     DUTCHMEN / FREEDOM SPIRIT     2009
Manufacturer: DUTCHMEN MANUFACTURING, INC. Mfr’s Report Date: JUN 02, 2010
NHTSA CAMPAIGN ID Number: 10V244000 N/A NHTSA Action Number: N/A
Component: EQUIPMENT:OTHER:LABELS
Potential Number of Units Affected: 100

FREIGHTLINER ( 10V247000 )

June 10, 2010

Vehicle Make / Model:     Model Year(s):
     FREIGHTLINER / MT55     2010-2011
Manufacturer: DAIMLER TRUCKS NORTH AMERICA Mfr’s Report Date: JUN 04, 2010
NHTSA CAMPAIGN ID Number: 10V247000 N/A NHTSA Action Number: N/A
Component: POWER TRAIN:AUTOMATIC TRANSMISSION

Pfizer Recalls Metronidazole Injection, Ciprofloxacin Injection, and Ondansetron Injection Bags Made by Claris Lifesciences Due to Non-Sterility

June 9, 2010

Pfizer Inc is voluntarily recalling Metronidazole, Ciprofloxacin and Ondansetron IV Products due to the presence of floating matter and non-sterility discovered by the manufacturer Claris Laboratories. Non-sterility of a product administered via the intravenous route has the potential to result in infections, which could be fatal, especially in patients who are immunocompromised. Metronidazole and Ciprofloxacin injections are intravenous antibiotics used to treat infections. Ondansetron injection is an intravenous product used to treat nausea and vomiting associated with chemotherapy or surgery. These products are supplied in plastic IV bags.

West-Ward Pharmaceuticals Recalls Ondansetron in 5% Dextrose Injection And Metronidazole Injection, USP Bags

June 9, 2010

West-Ward Pharmaceuticals Inc., of Eatontown, NJ, is voluntarily recalling all lots of Claris LifeSciences Inc. manufactured Ondansetron in 5% Dextrose Injection, supplied in 32mg/50mL Single-Use Plastic Bag Containers and Metronidazole Injection 500mg/100ml USP in Flexible IV Plastic Bag Containers. Claris recently received reports of the presence of floating matter and non-sterility in Ondansetron and Metronidazole. Non-sterile products administered intravenously may cause infections which could be fatal especially in patients who are immuno-compromised.

Defibtech Announces a Voluntary Recall of DBP-2800 Battery Packs used in the Lifeline AED and ReviveR AED

June 9, 2010

Contact:
Technical Support:
Tel: 1-877-453-4507, 1-203-453-4507
Media Inquiries:
Ray Valek,
Tel: 708-352-8695
ray@defibtech.com

Bayside Furnishings Recalls to Repair Youth Beds Sold at Costco Due to Entrapment Hazard

June 9, 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.

KEYSTONE ( 10V241000 )

June 9, 2010

Vehicle Make / Model:     Model Year(s):
     KEYSTONE / RESIDENCE     2010-2011
Manufacturer: KEYSTONE RV COMPANY Mfr’s Report Date: JUN 01, 2010
NHTSA CAMPAIGN ID Number: 10V241000 N/A NHTSA Action Number: N/A
Component: EQUIPMENT:RECREATIONAL VEHICLE
Potential Number of Units Affected: 43

BAD BOY ( 10V231000 )

June 9, 2010

Vehicle Make / Model:     Model Year(s):
     BAD BOY / CLASSIC LSV     2009-2010
Manufacturer: BAD BOY ENTERPRISES, LLC Mfr’s Report Date: MAY 28, 2010
NHTSA CAMPAIGN ID Number: 10V231000 N/A NHTSA Action Number: N/A
Component: VEHICLE SPEED CONTROL:ACCELERATOR PEDAL

FORD ( 10V243000 )

June 9, 2010

Vehicle Make / Model:     Model Year(s):
     FORD / E150     2007-2009
     FORD / E250     2007-2009
     FORD / E350     2007-2009
Manufacturer: MOBILITY TRANSPORTATION SERVICES Mfr’s Report Date: JUN 03, 2010

FORD ( 10V242000 )

June 9, 2010

Vehicle Make / Model:     Model Year(s):
     FORD / E150     2007-2009
     FORD / E250     2007-2009
     FORD / E350     2007-2009
Manufacturer: MOBILITY TRANSPORTATION SERVICES Mfr’s Report Date: JUN 03, 2010

KEYSTONE ( 10V239000 )

June 9, 2010

Vehicle Make / Model:     Model Year(s):
     KEYSTONE / COUGAR HIGH COUNTRY     2010-2011
Manufacturer: KEYSTONE RV COMPANY Mfr’s Report Date: JUN 01, 2010
NHTSA CAMPAIGN ID Number: 10V239000 N/A NHTSA Action Number: N/A
Component: STRUCTURE:BODY

Eastern Fish Recalls Hannaford and Bloom Private Brand Frozen Raw Extra Jumbo Shrimp Packaged in 16 oz. Bags, Product of Mexico

June 8, 2010

Eastern Fish is alerting consumers that Hannaford Supermarkets and Bloom brands of frozen raw extra jumbo (16/20) shrimp in 16 oz packages, as well as these brands of shrimp from the full-service seafood cases, labeled as product of Mexico, sold May 4 through June 4 at Hannaford Supermarkets and sold April 8 through June 4 at Bloom grocery stores, are subject to a voluntary recall because the products may contain undeclared sulfites. People who have an allergy or sensitivity to sulfites risk an allergic reaction if they consume these products.

Sagent Pharmaceuticals Recalls All Lots of Ondansetron in 5% Dextrose Injection, 32 mg/50 mL Manufactured by Claris Lifesciences

June 8, 2010

Sagent Pharmaceuticals, Inc. announced the voluntary nationwide recall of all lots of ondansetron injection in 5% dextrose 32mg / 50 mL (NDC number 25021-776-50) manufactured by Claris Lifesciences and distributed by Sagent. The lot numbers being recalled are: A090309, A090310, A090311 and A090312, which were distributed to hospitals, wholesalers and distributors nationwide from August 2009 through May 2010. Ondansetron injection is an intravenous product used to treat nausea and vomiting associated with chemotherapy or surgery and is supplied in a single dose plastic container.

CHRYSLER ( 10V235000 )

June 6, 2010

Vehicle Make / Model:     Model Year(s):
     CHRYSLER / TOWN & COUNTRY     2008-2009
     DODGE / GRAND CARAVAN     2008-2009
Manufacturer: CHRYSLER GROUP LLC Mfr’s Report Date: JUN 01, 2010
NHTSA CAMPAIGN ID Number: 10V235000 N/A NHTSA Action Number: N/A

2008-2009 Dodge Caravan and Town & Country Vehicles

June 6, 2010

Vehicle Make / Model:     Model Year(s):
     CHRYSLER / TOWN & COUNTRY     2008-2009
     DODGE / GRAND CARAVAN     2008-2009
Manufacturer: CHRYSLER GROUP LLC Mfr’s Report Date: JUN 01, 2010
NHTSA CAMPAIGN ID Number: 10V235000 N/A NHTSA Action Number: N/A

DODGE ( 10V234000 )

June 6, 2010

Vehicle Make / Model:     Model Year(s):
     DODGE / CALIBER     2007
     JEEP / COMPASS     2007
Manufacturer: CHRYSLER GROUP LLC Mfr’s Report Date: JUN 01, 2010
NHTSA CAMPAIGN ID Number: 10V234000 PE10012 NHTSA Action Number: PE10012

2007 Jeep Compass Recalls

June 6, 2010

Vehicle Make / Model:     Model Year(s):
     DODGE / CALIBER     2007
     JEEP / COMPASS     2007
Manufacturer: CHRYSLER GROUP LLC Mfr’s Report Date: JUN 01, 2010
NHTSA CAMPAIGN ID Number: 10V234000 PE10012 NHTSA Action Number: PE10012

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