Pacific Coast Fruit Company, Portland, Oregon is voluntarily recalling multiple types of fresh cut processed items based on the potential contamination of Salmonella Braenderup, an organism which can cause serious and sometimes life-threatening for infants, older people, pregnant woman and people with weakened immune systems. The most common symptoms of Salmonella are diarrhea, abdominal cramps and fever, which develop within eight to 72 hours of eating contaminated food.
Taylor Farms New Jersey Recalls Products Containing Daniella Brand Mangoes
Taylor Farms New Jersey is voluntarily recalling specific code dates of the following products due to containing Daniella Brand mangoes or potentially being processed on common equipment with the Daniella Brand mangoes. Daniella Brand mangoes were identified by the CFIA as having the potential to be contaminated with Salmonella Braenderup, and are subject to a prior recall posted by CFIA and FDA.
Winn-Dixie Issues Voluntary Recall On Cut Fruit Produced By Renaissance Food Group – Tropical Salsa, Fruit Burst, Island Medley Due To Possible Heath Risk
Winn-Dixie today announced an immediate voluntary recall of select cut fruit produced by Renaissance Food Group. The products are being recalled as a precaution because they contain a mango ingredient that has the potential of being contaminated with Salmonella braenderup.
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Salmonella Press Release for Milk Replacer
Quality Feed, Inc. recalls milk replacer because of possible salmonella health risk. Quality Feed, Inc. of Dousman, WI is recalling milk replacer that was shipped between January 31, 2012 and March 31, 2012 because it has the potential to be contaminated with Salmonella.
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Respironics California, Inc., Voluntary Recall Notification Of A Limited Number Of Respironics V60 Ventilators
Respironics California, Inc., a division of Philips Healthcare announced
today that it has completed notifying its United States customers of a voluntary recall of
116 Respironics V60 Ventilators in the United States and has confirmed that 33 have
already been updated. The recall was initiated on July 31, 2012 to address a
manufacturing issue that may have affected these ventilators.
FDA approves new treatment for a type of late stage prostate cancer
The U.S. Food and Drug Administration today approved Xtandi (enzalutamide) to treat men with late-stage (metastatic) castration-resistant prostate cancer that has spread or recurred, even with medical or surgical therapy to minimize testosterone.
BI-LO Issues Voluntary Recall on Daniella Brand Mangoes Due to Possible Health Risk
Today BI-LO announced an immediate voluntary recall on whole Daniella brand mangoes sold with a universal product code (UPC) of 0-00000-04051 in stores between July 12 and Aug. 27, 2012. The recalled mangoes, a product of Mexico, were sold as individual fruit and can be identified by the Daniella brand sticker.
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Stop & Shop Alerts Customers to Voluntary Recall of Splendid Products LLC Daniella Mangos
The Stop & Shop Supermarket Company, LLC, following a voluntary recall by Splendid Products announced it removed from sale Daniella mangos due to possible salmonella contamination. The following product, purchased between July 12 and August 24, 2012 is included in this recall: Daniella mangos, PLU 4959
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World Foods, LLC, Florida initiates voluntary recall of cut fruit and salsa products that contain Daniella Mangoes
World Foods, LLC is initiating a voluntary, precautionary recall on various products it distributes to retail supermarkets that contain mangoes associated with the Splendid Products recall of Daniella Brand Mangoes with the potential to be contaminated with Salmonella.
Brand New Energy Announces Voluntary Recall of Dietary Supplement EphBurn 25 Due to Possible Health Risk
Brand New Energy ("BNE"), dietary supplement re-sale distributor, is recalling all lot codes of EphBurn 25. The recall was initiated on August 28, 2012, after notification by the Food and Drug Administration (FDA) to a third-party retailer which purchased EphBurn 25 that one lot of EphBurn 25 was sampled by the FDA and found to contain ephedrine alkaloids, making it an unapproved drug.