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  2. How To Find Out If Your State Is Affected By The FDA’s ...

    www.aol.com/lifestyle/state-affected-fda-massive...

    Recalled Diet Coke has a best by date of 01/29/24, lot no. JAN2924MBD3, and UPC code 49000028911. Recalled Fanta Orange has the best by date of 07/29/24, lot no. JUL2924MBD3, and UPC code 49000030730.

  3. The 28 sodas, juices and other drinks recalled by the FDA ...

    www.aol.com/28-sodas-juices-other-drinks...

    Drink recall 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 ...

  4. FDA recalls soda company's drinks sold at restaurants for ...

    www.aol.com/fda-recalls-soda-companys-drinks...

    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 ...

  5. FDA recall policies - Wikipedia

    en.wikipedia.org/wiki/FDA_recall_policies

    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.

  6. Drug recall - Wikipedia

    en.wikipedia.org/wiki/Drug_recall

    A drug recall removes a prescription or over-the-counter drug from the market. Drug recalls in the United States are made by the FDA or the creators of the drug when certain criteria are met. When a drug recall is made, the drug is removed from the market and potential legal action can be taken depending on the severity of the drug recall. [1]

  7. Food and Drug Administration Safety and Innovation Act

    en.wikipedia.org/wiki/Food_and_Drug...

    The Food and Drug Administration Safety and Innovation Act of 2012 (FDASIA) is a piece of American regulatory legislation signed into law on July 9, 2012.It gives the United States Food and Drug Administration (FDA) the authority to collect user fees from the medical industry to fund reviews of innovator drugs, medical devices, generic drugs and biosimilar biologics.

  8. FDA issued over 20 recalls in August. Check this list to see ...

    www.aol.com/fda-issued-over-20-recalls-182642974...

    The FDA has announced over 20 recalls across the U.S., including food items, cosmetics, drugs, dietary supplements, and medical devices.

  9. Regulation of food and dietary supplements by the U.S. Food ...

    en.wikipedia.org/wiki/Regulation_of_food_and...

    This policy was later challenged in court following FDA approval of a food coloring manufactured with a compound known to be carcinogenic, after separate testing indicated that the food coloring itself did not cause cancer in test animals. The United States Court of Appeals for the Sixth Circuit upheld the FDA's approval of the food coloring. [36]