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Orlando Sentinel – FDA Food & Product Recalls & Updates

Posted by 4love2love on June 24, 2011

Tip of one of the knives can protrude through the bottom, posing a laceration hazard

The U.S. Consumer Product Safety Commission and Health Canada, in cooperation with the firm named below, today announced a recall of about 217,000 in Calphalon Contemporary Cutlery Knife Sets in the United States and about 300 sets in Canada. The tips of the 8-inch slicing knife and/or the 8-inch bread knife can protrude through the bottom slot row on the wooden block holder, posing a laceration hazard. Calphalon has received one report of a cut finger injury. Consumers should stop using recalled products immediately unless otherwise instructed. It is illegal to resell or attempt to resell a recalled consumer product.

 

Continue reading Recall alert: Calphalon knife block sets can pose laceration hazard »

 

 

Mediterranean Thin Crust Pizza

Kashi is recalling approximately 11,000 cases of frozen pizzas, including Mediterranean Thin Crust Pizza, Roasted Vegetable Thin Crust Pizza, and Mushroom Trio and Spinach Thin Crust Pizza due to possible plastic fragments in an ingredient in the pizza crusts.

The impacted products include the following individually packaged pizzas:

Kashi Mediterranean Thin Crust Pizza packaged in a 12.7 ounce box and marked with UPC Code 1862732905 3 and Best If Used Before date of either May10 12NU, May18 12NU, or May19 12NU;
Kashi Roasted Vegetable Thin Crust Pizza packaged in a 12.2 ounce box and marked with UPC Code 1862737342 1 and Best If Used Before date of either May09 12NU or May14 12NU;
Kashi Mushroom Trio and Spinach Thin Crust Pizza packaged in an 11.9 ounce box and marked with UPC Code 1862737344 5 and Best If Used Before date of May17 12NU.
No other Kashi frozen pizzas or other products are included in the recall, and no consumer complaints have been reported. The products were distributed nationwide through U.S. retail grocery stores.

 

Continue reading Recall alert: Select Kashi pizzas may contain plastic fragments »

 

 

Nielsen-Massey: Vanilla paste recall was unnecessary 

 

A voluntary recall of Nielsen-Massey Vanillas’ Madagascar Bourbon Pure Vanilla Bean Paste has been found to be based on a false-positive Listeria reading reported by the company’s outside testing laboratory. Subsequent investigations and further tests by the FDA, the outside lab in question and another independent lab brought in to re-verify the results, all came back negative. There were no positive results in any raw material used or for any of the equipment used in the process. Additionally, the other independent lab and the FDA laboratory, using the exact same gallon bottle of Paste which tested positive initially, found no trace of Listeria whatsoever. As the FDA did not have any findings as a result of their investigation, no Form 483 was issued.

 

Continue reading Nielsen-Massey: Vanilla paste recall was unnecessary »

 

 

Recall alert: Nielsen-Massey Madagascar Vanilla Bean Paste 

 

UPDATE! Recall  found to be unneededNielsen-Massey Vanillas, Inc. of Waukegan, Illinois is voluntarily recalling lot No. 11123 of itsNielsen-Massey Madagascar Bourbon Pure Vanilla Bean Pastebecause it has the potential to be contaminated with Listeria monocytogenes, an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. This recall extends nationally to all states of the United States and outside the United States in Canada. This recall extends to all levels of distribution, including the retail level. The recalled product was offered in translucent plastic one-gallon- and one-quart-size containers, through a variety of distribution channels including direct delivery to business customers, distributors and retail sales. There have been no reports of illness related to Nielsen-Massey’s Madagascar Bourbon Pure Vanilla Bean Paste.

 

Continue reading Recall alert: Nielsen-Massey Madagascar Vanilla Bean Paste »

 

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