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On November 6, the U.S. Food & Drug Administration issued a recall on Diet Coke, Sprite, and Fanta Orange sold in three states due to a "potential foreign material." United Packers, LLC initiated ...
The FDA has recalled 28 beverages so far in 2024, The Daily Mail reported. All but four of the drinks were recalled because they had drugs, bacteria or harmful chemicals in them that the company ...
The recall affects four of the company's drinks: Pink Lemonade, Cola Flavoring Base, Yellow Lemonade, and Yellow Lemonade X. These beverages, sold in 1- and 5-gallon quantities, are distributed to ...
The 17 November 2010 [1] United States ban on caffeinated alcoholic drinks is a ban which prevents the marketing and distribution of any prepackaged caffeinated alcoholic drink. Such a ban was discussed as a result of multiple cases of alcohol poisoning and alcohol -related blackouts among users of such drinks.
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.
If the firm markets other FDA-regulated products and the issue(s) affect marketed products—or the inspection extended to marketed products included on the FDA 483, then they may issue a Warning Letter These include the following statement: "Due to the deficiencies listed on the attached FDA 483 we are recommending to the center that approval ...
Yellow Lemonade X drinks, lot/unit number 1-015, for undeclared FD&C Yellow No. 5 Cola flavoring base , lot/unit numbers 9-330, 9-348, 1-013, 1-036, 1-097, for undeclared sulfites
If food is adulterated, FDA and FSIS have a broad array of enforcement tools. These include seizing and condemning the product, detaining imported product, enjoining persons from manufacturing or distributing the product, or requesting a recall of the product. Enforcement action is usually preceded by a Warning Letter from the FDA to the ...