Friday, September 03, 2010

Lead Recalls

Below is a list of lead based recalls. A large number of products have recently been recalled due to high levels of unsafe lead.

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1-25 of 291 Recalls  

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  • Sorry. Image not available.
    Torn & Glasser of Rancho Dominguez, CA is recalling its 3.75lb (#10) cans of “Mixed Nuts Fancy, No Peanuts” marked with lot numbers 0980 and 1940 on the outer case label and bottom lid due to undeclared peanuts. People who have allergies to peanuts run the risk of serious or life-threatening allergic reaction if they consume these products. The recalled “Mixed Nuts Fancy, No Peanuts” were distributed in CA, WA and HI. This was distributed through a wholesale distribution outlet. The product comes in a sealed, 3.75lb #10 style can marked with lot numbers 0980 and 1940 on the outer case label and bottom lid. The UPC is 072488980761.

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  • Sorry. Image not available.
    Sparboe Farms is voluntarily recalling shell eggs produced by Wright County Egg and Hillandale Farms which were packaged by Sparboe Farms, because they have the potential to be contaminated with Salmonella. Salmonella is an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems.Healthy persons infected with Salmonella often experience fever, diarrhea, nausea, vomiting and abdominal pain. In rare circumstances, infection with Salmonella can result in the organism getting into the bloodstream and producing more severe illnesses such as arterial infections, endocarditis, or arthritis.

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    The following statement was released by officials of Wright County Egg regarding its voluntary recall of some shell eggs in cooperation with the US Food and Drug Administration's (FDA). Wright County Egg of Galt, Iowa is adding one California-distributed brand label – Cardenas Market – to its voluntary recall of August 13, 2010 of specific Julian dates of shell eggs produced by their farms because they have the potential to be contaminated with Salmonella...

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  • Sorry. Image not available.
    Integra LifeSciences Corporation, Plainsboro, New Jersey, has initiated a worldwide recall of the NeuroBalloon Catheter. There were a total of 1,924 units distributed, 258 in the United States of America 1,586 in the European Union and 80 in countries. A total of eight (8) complaints regarding the inflation or deflation of the NeuroBalloon Catheter were received by Integra. All complaints occurred outside the United States. No patient injuries have been reported. As a result of the investigation performed by Integra, it was determined that this condition could exist during pre-implant testing or during the procedure. Integra issued a voluntary recall of the affected lots of the NeuroBalloon Catheter on July 2, 2010.

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Note: Our database contains safety recalls issued by the Consumer Product Safety Commission (CPSC), the National Highway Traffic Safety Administration (NHTSA) and the Food and Drug Administration (FDA). For a complete release on alerts, recalls, or press releases issued to the public please visit the appropriate website. A compiled list of these websites can be found in the links section of this website.

Disclaimer: This information presented on this website is being provided as a courtesy. We've worked really hard to keep the records in our database as current and accurate as possible. In the unlikely event that our automated system fails, or contains bugs that incur incomplete records we take no responsibility. We take no responsibility for the information presented on this website. For a complete release on recalled products please visit the appropriate websites.