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Unilever announced today a massive recall of Slim-Fast diet drinks, citing concerns about the presence of Bacillus cereus, a bacteria that can cause diarrhea, nausea, and vomiting. Wait: Hasn't ...
A recall of the diet drinks is. Every can of the diet aid Slim-Fast sold in the United States is being recalled after dangerous bacteria was discovered by the manufacturer during a routine ...
Dieters who drink Slim-Fast shakes to curb their appetites may find the product works rather differently than planned -- at least that's what the maker of the popular ready-to-drink nutritional ...
SlimFast was started in 1977 as a product line of the Thompson Medical Company, founded in the 1940s by S. Daniel Abraham.The product was rolled out nationwide in a marketing campaign that began on July 11, 1977 for "a fat-free, carbohydrate-free, animal-based fortified cherry-flavored protein supplement formula" that promised to make purchasers "feel better, cleaner, stronger and healthier.
Abraham founded Thompson Medical, which introduced the SlimFast line of diet products in the late 1970s. [6] Abraham made Thompson Medical private in 1988; Unilever acquired Slim-Fast for $2.3 billion in 2000. [7] [8] As of October 2016, he had an estimated wealth of US$2.1 billion. [1]
Nutrisystem's initial product in 1972 was a liquid protein diet, but the company changed its offering after Slim-Fast came to prominence in that market. [1]The company originally offered weight loss counseling and products in brick and mortar centers, but in 1999, Nutrisystem moved to a direct-to-consumer business model, selling its products and programs on the Internet and by telephone.
Coca-Cola issued a recall of almost 2,000 cases of Diet Coke, Sprite and Fanta Orange after finding the cans may contain "foreign material." Skip to main content. Sign in. Mail. 24/7 Help ...
FDA's role under the guidelines is to monitor company recalls and assess the adequacy of a firm's action. After a recall is completed, FDA makes sure that the product is destroyed or suitably reconditioned and investigates why the product was defective. Generally, FDA accepts reports and other necessary recall information submitted by e-mail.