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Recalled Food List for the Week of July 16th

Good Health Inc Issues Recall for Vialipro Dietary Supplement

Good Health Inc is recalling the dietary supplement Vialipro, sold for sexual enhancement, because an FDA lab analysis found that the product may contain sulfoaildenafil, an analogue of an FDA approved drug used in the treatment of male erectile dysfunction.  The presence of this ingredient makes the supplement an undeclared drug.  Sulfoaildenafil can interact with some prescription drugs, such as nitroglycerin, lowering blood pressure to dangerous levels.  10 lot numbers are included in the recall and can be found at the link above.

Slim-30 Herb Supplement Recalled Due to Undeclared Drug Ingredient

J&H Besta Corp of Hicksville NY has been informed by the FDA that lab analysis of the Slim-30 Herb Supplement contains traces of sibutramine, a drug used as an appetite suppressant.  The FDA advises that this product poses a threat to consumers because sibutramine can increase blood pressure and/or pulse rate in some patients and could present a significant risk to those with coronary artery disease, congestive heart failure, arrhythmias or stroke.  The affected lot/code being recalled is 032009, bearing the UPC code 8 31457 005009 2.  It was sold to distributors and retail stores nationwide and via internet sales.

Adverse reactions to Slim-30 should be reported to the FDA’s MedWatch Safety Information and Adverse Event Reporting Program at www.fda.gov/medwatch.

D&M Smoked Fish Issues Alert on Schmaltz Herring

D&M Smoked Fish Inc, located in Queens NY, is recalling Haifa brand vacuum packaged Schmaltz Herring with lot number 168 because the product was found to be uneviscerated, the sale of which is prohibited under New York State Agriculture and Markets regulations because Clostridium Botulinum spores are more likely to be concentrated in the viscera than any other portion of the fish.  No illnesses have been reported.  Customers can return the product to place of purchase for a refund or contact D&M at 718-523-8899.

Diamond USA Inc Recalls Dry Apricot Rolled Due to Undeclared Sulfites

Diamond USA has recalled its 1 pound packages of Dry Apricot Rolled, code #01-12-2010, because it may have undeclared sulfites which can cause a reaction in those with sensitivities to the compound.  These products were distributed in New York, New Jersey, Virginia, and California to retail stores.  No illnesses have been reported.  Consumers can return the product to the place of purchase for a full refund or contact the company at 718-938-0345.

Fresh Express Recalls Expired Romaine Lettuce

Fresh Express is voluntarily recalling certain Romaine lettuce salad products with expired Use-by dates of July 9th through 12th.  The packages also can be identified by an “S” in the product code.  The lettuce has the potential to be contaminated with E. coli, but no illnesses have been reported.  Although the product is expired, some consumers may still have the lettuce in their refrigerators.  Customers can contact Fresh Express for more information by calling 800-242-5472 Monday through Friday 5am to 8pm PT.

QFC Recalls Broccoli Raisin Salad for Undeclared Allergen

Seattle’s Quality Food Center (QFC) is recalling select containers of Broccoli Raisin Salad because they may contain walnuts that are not on the label.  The containers were sold in Oregon and Washington in the deli service department on July 10.  Customers should return the products for a full refund or contact www.qfc.com/recalls for more information.

For more information about US Food and Drug Administration Recalls, or to receive your own RSS feed, visit www.fda.gov

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