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.

Name of Product: Honda Snowblowers

Units: About 18,500

Importer: American Honda Motor Co. Inc., of Torrance, Calif.

Hazard: The fuel tank joint and O-ring located on the underside of the fuel tank can seep or drip fuel over time, posing a fire hazard.

Incidents/Injuries: Honda has received 90 reports of fuel either seeping or dripping. No fires have been reported.

Description: This recall involves Honda snowblowers with model numbers and frame serial numbers listed below. The snowblowers are red and black. The frame serial number is located on the rear of the machine just below the engine. The name Honda and the model number are located on the side of the front scoop.

Model Frame Serial Number
HS724 SZBE-1037913 through 1046577
HS928 SZAS-1151080 through 1169012
HS1132 SZBF-1018734 through 1025998

 

Sold at: Honda Power Equipment dealers nationwide from April 2005 through November 2010 for between $2,000 and $3,400.

Manufactured in: Japan

Remedy: Consumers should immediately stop using the recalled snowblowers and contact any Honda Power Equipment dealer to arrange for a free fuel tank joint and O-ring replacement. Registered owners of the recalled snowblowers will be mailed a notice.

Consumer Contact: For additional information, contact Honda at (888) 888-3139 between 8:30 a.m. and 5 p.m. ET Monday through Friday, or visit the firm’s website at http://www.hondapowerequipment.com/products/recalls/

What Happened

All unexpired lots of certain over-the-counter (OTC) liquid medicines for infants and children have been voluntarily recalled because some might not meet required quality standards.

The recall has been issued in the Unites States, Canada, Dominican Republic, Dubai (UAE), Fiji, Guam, Guatemala, Jamaica, Kuwait, Panama, Puerto Rico, and Trinidad & Tobago by Johnson & Johnson’s McNeil Consumer Healthcare in consultation with the U.S. Food and Drug Administration (FDA).

What This Means

This latest recall includes eight OTC medicines in 43 different flavors and sizes, including:

  1. Tylenol Infants’ Drops
  2. Children’s Tylenol Suspensions
  3. Children’s Tylenol Plus Suspensions
  4. Motrin Infants’ Drops
  5. Children’s Motrin Suspensions
  6. Children’s Motrin Cold Suspensions
  7. Children’s Zyrtec Liquids in Bottles
  8. Children’s Benadryl Allergy Liquids in Bottles

McNeil is recalling the products because some might contain more of the active drug ingredient than specified, while others might have inactive ingredients that might not meet internal testing requirements, or may contain tiny particles. Information about the specific lots recalled is on McNeil’s recall website; affected product NDC numbers are on the label of the bottle above the brand name.

The company advises consumers to stop using these products immediately, although it believes that the potential for serious medical problems is remote. No adverse medical reactions have been reported.

The company is investigating the Fort Washington, PA, plant where the recalled products were made to ensure there are no other problems, and plans to take corrective actions before restarting production.

Where These Products Were Sold

Drugstores, grocery stores, and other retailers in the United States, Canada, Dominican Republic, Dubai (UAE), Fiji, Guam, Guatemala, Jamaica, Kuwait, Panama, Puerto Rico, and Trinidad & Tobago.

What to Do Next

Check the firm’s recall website to see if you have any packages included in the recall. If so, stop using them immediately and contact McNeil for a refund (either for the average product retail price or a coupon for a free replacement when the product is available again).

Should your child need medicine included in the recall, the FDA advises that generic versions of these products are widely available and not affected by the recall. Check the product labeling for use in children, and if you have questions, talk to your doctor or pharmacist. Do not give kids adult-strength medicine, as it may result in serious harm.

For More Information

Recall date: April 30, 2010

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Excerpt from:
Synthes USA, Ti Synex II Vertebral Body Replacement – Class I Recall

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Dr. Margaret Hamburg, Commissioner of Food and Drugs, today sent a letter to America’s doctors thanking them for their efforts during the 2009 H1N1 influenza outbreak and providing information on the safety of the 2009 H1N1 vaccines.

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Product, used during cardiopulmonary bypass procedures, may spontaneously rupture during surgery.

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Read the original here:
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Updated code is a model for state, city, county, tribal, territorial agencies and industry. The Food and Drug Administration today announced the publication of the new FDA Food Code, a model code and reference document that provides a scientifically sound technical and legal basis for regulating the retail and food service segment of the food industry. The 2009 FDA Food Code is a key component of the President’s overall public-health-focused food safety framework for maintaining a safe food supply.

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The U.S. Food and Drug Administration is issuing this health alert to warn consumers not to use Pig Ears and Beef Hooves pet treats manufactured by Pet Carousel because the products may be contaminated with Salmonella

Go here to see the original:
FDA Health Alert for Certain Pet Treats Made by Pet Carousel

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