Latest news with #ZeroSugar
Yahoo
12-06-2025
- Health
- Yahoo
Dr. Pepper zero recall upgraded in Georgia, South Carolina
SAVANNAH, Ga. (WSAV) — Dr. Pepper is recalling over 19,000 cases of their Zero Sugar soda in three Southern states. The recalled sodas, which are labeled as having zero sugar, actually contained the full sugar product. Because the cans were mislabeled as having zero sugar, they could cause a health risk for diabetics or others who need to limit their sugar intake or avoid it altogether. The voluntary recall was initiated for Zero Sugar Dr. Peppers with a best by date of Feb. 16, 2026, in Georgia, Florida and South Carolina. The sodas were sold in 12-pack and 24-pack cases of 12-ounce cans. The affected product code is XXXXRS05165. The FDA upgraded the recall to Class II last week due to the health risks associated. If you purchased Dr Pepper drinks matching these descriptions, you can return them to the place you purchased them for a full refund or safely dispose of them. Copyright 2025 Nexstar Media, Inc. All rights reserved. This material may not be published, broadcast, rewritten, or redistributed.
Newsweek
08-06-2025
- Health
- Newsweek
Dr Pepper Recall Issued After Sugar Mix Up in Thousands of Cans
A recall has been issued for thousands of cases of Dr Pepper Zero Sugar that were mislabeled and contained the full-sugar product, according to the U.S. Food and Drug Administration (FDA). The products were distributed to retailers in Florida, Georgia, and South Carolina. Newsweek contacted Keurig Dr Pepper, which owns the product in the United States, and PepsiCo, which bottled the beverages, for comment via email outside of regular working hours. Why It Matters This mislabeling poses potential health risks to consumers, particularly for individuals managing conditions like diabetes or those monitoring their sugar intake The FDA has issued a Class II risk classification for the recall, indicating that the consumption of the mislabeled products may cause temporary or medically reversible adverse health consequences. What To Know The FDA said the company-initiated recall affects 19,203 cases of Dr Pepper Zero Sugar 12-fluid ounce cans, sold in 12-pack and 24-pack cartons. The affected cans were produced at a Pepsi bottling facility in Jacksonville, Florida, which is licensed to manufacture Keurig Dr Pepper products, according to the FDA. The affected products have the product code XXXXRS05165, and a best-by date of February 16, 2026. The recall was initiated on May 23, 2025, and the FDA classified it as a Class II recall on June 5, 2025. A can of regular Dr Pepper contains 39 grams of sugar, while the Zero Sugar version has zero grams, but contains the artificial sweeteners aspartame and acesulfame potassium. There were 241 FDA food and beverage recalls in 2024, which was an increase of eight percent from the previous year, according to a report published by the nonprofit Public Interest Research Group. Undeclared allergens or ingredients was the single biggest cause for recalls that year. Last year, Dr Pepper tied with Pepsi to become the second most popular soda in the U.S. after Coca Cola, according to data from Beverage Digest. What Happens Next The FDA and Dr Pepper are working to ensure that all affected products are removed from store shelves promptly. Consumers in the affected states should remain vigilant and check their purchases to ensure they have not bought the mislabeled product.
Yahoo
06-06-2025
- Health
- Yahoo
FDA Announces Recall on More Than 19,000 Cases of Dr Pepper for Mislabeling
According to a notice posted by the U.S. Food & Drug Administration (FDA), more than 19,200 12- and 24-pack cases of Dr Pepper Zero Sugar have been recalled. The recall was initiated after the soda, which is labeled as 'zero sugar,' was found to contain full sugar. The recalled cases of Dr Pepper Zero Sugar were produced by Jacksonville, Florida-based Pepsi Beverages Company, which is licensed to manufacture Keurig Dr Pepper-owned products including Dr Pepper. The soda was distributed to retailers in three states: Florida, Georgia, and South Carolina. To identify if you have the recalled Dr Pepper, you should check for the following information: 12- or 24-pack carton cases of 12-fluid ounce aluminum cans of Dr Pepper, Zero Sugar Prod Code: XXXXRS05165 "Best By" Date: Feb. 16, 2026 The recall was initiated on May 23, 2025, with the FDA classifying it as a Class II recall—meaning drinking the product could cause 'temporary or medically reversible adverse health consequences'—on June 5, 2025. Because Pepsi Beverages Company initiated the recall at the end of May, it is likely that the products have been pulled from retailer shelves by now; however, you should check to code number just to be sure. No other Dr Pepper Zero Sugar cases or Dr Pepper products are impacted by this recall. If you have the recalled Dr Pepper Zero Sugar and are someone who is monitoring and controlling their sugar intake for medical reasons, it may not be safe to consume the soda. If that's the case, you should throw it away or return it to the original place of purchase for a full refund or replacement. If you are not monitoring your sugar intake, you do not need to do anything regarding this recall. The product was recalled for mislabeling, not because it is inherently harmful to consume. The full-sugar soda just may have a different flavor than anticipated. However, if you do wish to receive the zero-sugar Dr Pepper that you intended to purchase, you can return it to the original place of purchase for a replacement or full refund. Read the original article on ALLRECIPES
Newsweek
06-06-2025
- Business
- Newsweek
Dr Pepper Recalled After Sugar Mix Up in Thousands of Cans
Based on facts, either observed and verified firsthand by the reporter, or reported and verified from knowledgeable sources. Newsweek AI is in beta. Translations may contain inaccuracies—please refer to the original content. A recall has been issued for thousands of cases of Dr Pepper Zero Sugar that were mislabeled and contained the full-sugar product, according to the U.S. Food and Drug Administration (FDA). The products were distributed to retailers in Florida, Georgia, and South Carolina. Newsweek contacted Keurig Dr Pepper, which owns the product in the United States, and PepsiCo, which bottled the beverages, for comment via email outside of regular working hours. Thousands of cases of Dr Pepper Zero Sugar have been recalled after they were mislabeled and contained the full-sugar product. Thousands of cases of Dr Pepper Zero Sugar have been recalled after they were mislabeled and contained the full-sugar It Matters This mislabeling poses potential health risks to consumers, particularly for individuals managing conditions like diabetes or those monitoring their sugar intake The FDA has issued a Class II risk classification for the recall, indicating that the consumption of the mislabeled products may cause temporary or medically reversible adverse health consequences. What To Know The FDA said the company-initiated recall affects 19,203 cases of Dr Pepper Zero Sugar 12-fluid ounce cans, sold in 12-pack and 24-pack cartons. The affected cans were produced at a Pepsi bottling facility in Jacksonville, Florida, which is licensed to manufacture Keurig Dr Pepper products, according to the FDA. The affected products have the product code XXXXRS05165, and a best-by date of February 16, 2026. The recall was initiated on May 23, 2025, and the FDA classified it as a Class II recall on June 5, 2025. A can of regular Dr Pepper contains 39 grams of sugar, while the Zero Sugar version has zero grams, but contains the artificial sweeteners aspartame and acesulfame potassium. There were 241 FDA food and beverage recalls in 2024, which was an increase of eight percent from the previous year, according to a report published by the nonprofit Public Interest Research Group. Undeclared allergens or ingredients was the single biggest cause for recalls that year. Last year, Dr Pepper tied with Pepsi to become the second most popular soda in the U.S. after Coca Cola, according to data from Beverage Digest. What Happens Next The FDA and Dr Pepper are working to ensure that all affected products are removed from store shelves promptly. Consumers in the affected states should remain vigilant and check their purchases to ensure they have not bought the mislabeled product.
Reuters
29-05-2025
- Business
- Reuters
Chobani beats class action over 'zero sugar' label
May 29 (Reuters) - Chobani escaped a proposed class action over claims its 'Chobani Zero Sugar' yogurt actually contains sugar, after an Illinois federal judge on Thursday said the labeling met U.S. Food and Drug Administration requirements. The lawsuit accused Chobani of misleading consumers by failing to count the allulose – a fruit-derived sweetener – in the sugar content of its 'Zero Sugar' products. U.S. District Judge John Tharp Jr. in Chicago said U.S. Food and Drug Administration regulations govern how the yogurt is labeled and outweigh state consumer protection laws about labeling. The agency has not definitively said whether allulose is counted as sugar in its regulation governing nutrition labels for food products, but it has said that it is not currently treating allulose as a sugar and won't go after companies that leave it out of their products' sugar content listed on the label, Tharp said. Tharp dismissed the claims brought by the named plaintiffs and the proposed class of nationwide consumers. Attorneys for Chobani did not immediately respond to requests for comment, nor did attorneys for the proposed class. Four shoppers from Illinois, Arizona and Kansas filed the lawsuit in 2023, claiming they were misled by the 'Zero Sugar' labeling on the yogurts. Allulose is a monosaccharide or simple sugar with a chemical structure similar to fructose, so it isn't 'zero sugar,' the shoppers said. The lawsuit, which brought claims under 37 states' consumer protection laws, sought damages and disgorgement of Chobani's profits, among other things. Chobani moved to dismiss the lawsuit, pointing to the FDA's statements on allulose. Allowing the lawsuit to move forward would deter the use of a sugar-substitute that the FDA believes could improve public health by reducing sugar consumption, the company said. Tharp agreed, saying that while the FDA hasn't issued its definitive statement on allulose, its comments on how it views allulose have expressly authorized the 'Zero Sugar' label. The case is Jason Franco et al v. Chobani LLC, U.S. District Court for the Northern District of Illinois, No. 1:23-cv-03047. For Chobani: Drew Tulumello of Weil, Gotshal & Manges; and Erik Ives of Fox Swibel Levin & Carroll For the plaintiffs: Yates French and Heather Kramer of Rathje Woodward; and Alexander Burke of Burke Law Offices
