Main Mobility Recalls 186 Vans of Various Models

July 18, 2009

Vehicle Make / Model:     Model Year(s):
     CHEVROLET / EXPRESS     2005-2009
     GMC / SAVANA     2005-2009
Manufacturer: MAIN MOBILITY, INC. Mfr’s Report Date: JUN 25, 2009
NHTSA CAMPAIGN ID Number: 09V272000 EQ08011 NHTSA Action Number: EQ08011

CHEVROLET ( 09V273000 )

July 18, 2009

Vehicle Make / Model:     Model Year(s):
     CHEVROLET / G3500     2005
     FORD / E-150     2006
Manufacturer: WEST TEXAS REHABILITATION CENTER Mfr’s Report Date: JUL 06, 2009
NHTSA CAMPAIGN ID Number: 09V273000 EQ08011 NHTSA Action Number: EQ08011

Texas Rehabilitation Center Wheelchair Lift Recall

July 18, 2009

Vehicle Make / Model:     Model Year(s):
     CHEVROLET / G3500     2005
     FORD / E-150     2006
Manufacturer: WEST TEXAS REHABILITATION CENTER Mfr’s Report Date: JUL 06, 2009
NHTSA CAMPAIGN ID Number: 09V273000 EQ08011 NHTSA Action Number: EQ08011

2005 Chevrolet G3500 Van

July 18, 2009

Vehicle Make / Model:     Model Year(s):
     CHEVROLET / G3500     2005
     FORD / E-150     2006
Manufacturer: WEST TEXAS REHABILITATION CENTER Mfr’s Report Date: JUL 06, 2009
NHTSA CAMPAIGN ID Number: 09V274000 EQ08011 NHTSA Action Number: EQ08011

West Texas Rehabilitation Center Truck Recall

July 18, 2009

Vehicle Make / Model:     Model Year(s):
     CHEVROLET / G3500     2005
     FORD / E-150     2006
Manufacturer: WEST TEXAS REHABILITATION CENTER Mfr’s Report Date: JUL 06, 2009
NHTSA CAMPAIGN ID Number: 09V274000 EQ08011 NHTSA Action Number: EQ08011

‘G Collection’ Mother’s Day and Valentine’s Day Gift Boxes Are Voluntarily Recalled

July 17, 2009

The ‘G Collection’ Mother’s Day and Valentine’s Day gift boxes that were available for purchase during limited holiday timeframes in 2009 are being recalled by Godiva Chocolatier, the distributor of the G Collection.

L A Weight Loss Recalls L A Hot Drinks Café Au Lait Because of Possible Health Risk

July 17, 2009

NOTE: More info about the LA Weight Loss Drink Recall Here.

Brookstone Pharmaceuticals Concentrated Acetaminophen Drop Recall

July 17, 2009

NOTE: More info about the Brookstone Pharmaceutical concentrated acetaminophen drops here.

Kesso Foods Recalls 8 oz. and 16 oz. Low Fat All Natural Plain 2% Greek Thick Yogurt: Salmonella Risk

July 17, 2009

Kesso Foods, Inc. of East Elmhurst, NY is voluntarily recalling 8 oz. and 16 oz. Kesso Foods Lowfat All Natural Plain 2% Greek Thick Yogurt. The affected product has a “SELL BY” date up to and including August 10, 2009. The yogurt is being recalled because it contains nonfat dried milk manufactured by the Plainview Milk Products Cooperative of Plainview, MN. The nonfat dried milk has been subject to an FDA recall due to potential Salmonella contamination. There have been no complaints or reports of illness reported to Kesso Foods, Inc. up to date. The voluntary recall of our product is a precaution to ensure our client safety.

Teva Pharmaceuticals USA Recalls Propofol Injectable Emulsion

July 17, 2009

Teva Pharmaceuticals and FDA notified healthcare professionals of a recall of Propofol Injectable Emulsion 10 mg/mL 100 mL vials, lot numbers 31305429B and 31305430B. The product lots identified are being recalled due to the presence of elevated endotoxin levels in some vials within these lot numbers. Teva has been notified of 41 propofol-treated patients who experienced post-operative fever, chills and other flu-like symptoms. Adverse health effects, such as fever, chills, or rigors, are possible with exposure to product with elevated levels of endotoxins. Serious adverse effects, such as disseminated intravascular coagulopathy, acute respiratory distress syndrome, shock, and death, are possible with exposure to product with high endotoxin levels.

Young You Corporation Recalls Weight Loss Pills Found to Contain an Undeclared Drug Ingredient

July 17, 2009

Young You Corporation has been informed by the Food and Drug Administration (FDA) that four weight loss dietary supplements sold and marketed by the firm contain an undeclared drug ingredient. FDA lab analyses of dietary supplements distributed by the company were found to contain undeclared Sibutramine, an FDA-approved drug used as an appetite suppressant for weight loss. The FDA has not approved the following products as drugs; therefore the safety and effectiveness of this product is unknown.

Evenflo Recalls Telephone Toys Due to Choking Hazard

July 17, 2009

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: EVENFLO SWITCH-A-ROO TELEPHONE TOYS

UNITS: ABOUT 25,000

Butterfly Chairs Recalled by Hobby Lobby Due to Fall Hazard

July 17, 2009

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: LEATHER BUTTERFLY CHAIRS

UNITS: ABOUT 500

Leather Shag Rugs Recalled by Chandra Rugs Due to Fire Hazard

July 17, 2009

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: ART COLLECTION LEATHER SHAG RUGS

UNITS: ABOUT 400

Children’s Hooded Jackets with Drawstrings Recalled by EMH Associates Due to Entrapment Hazard

July 17, 2009

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: HOODED JACKETS

UNITS: ABOUT 4,400

Steam Cleaners Recalled by Thane International Due to Shock and Burn Hazards

July 17, 2009

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: H2O MOP STEAM CLEANERS

UNITS: ABOUT 580,000

GLAVAL ( 09V266000 )

July 17, 2009

Vehicle Make / Model:     Model Year(s):
     GLAVAL / CONCORDE     2005
Manufacturer: GLAVAL BUS DIVISION Mfr’s Report Date: JUL 10, 2009
NHTSA CAMPAIGN ID Number: 09V266000 PE09004 NHTSA Action Number: PE09004
Component: SERVICE BRAKES, HYDRAULIC:FOUNDATION COMPONENTS

Harley Davidson Recalls 1,759 FLTRSE3 2009 Motorcycles

July 17, 2009

Vehicle Make / Model:     Model Year(s):
     H-D / FLTRSE3     2009
Manufacturer: HARLEY-DAVIDSON MOTOR COMPANY Mfr’s Report Date: JUL 08, 2009
NHTSA CAMPAIGN ID Number: 09V267000 N/A NHTSA Action Number: N/A
Component: WHEELS
Potential Number of Units Affected: 1759

FORD ( 09V271000 )

July 17, 2009

Vehicle Make / Model:     Model Year(s):
     FORD / E-250     2006
     FORD / E-350     2005
Manufacturer: FREEWHEEL MOBILITY Mfr’s Report Date: JUN 25, 2009
NHTSA CAMPAIGN ID Number: 09V271000 EQ08011 NHTSA Action Number: EQ08011

FORD ( 09V275000 )

July 17, 2009

Vehicle Make / Model:     Model Year(s):
     FORD / E-250     2006
     FORD / E-350     2005
Manufacturer: FREEWHEEL MOBILITY Mfr’s Report Date: JUN 25, 2009
NHTSA CAMPAIGN ID Number: 09V275000 EQ08011 NHTSA Action Number: EQ08011

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