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Jacksonville Pepsi Distributor Issues Dr. Pepper Recall

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Dr. Pepper Zero Sugar cans with a recall notice displayed on a shelf.

News Summary

A Jacksonville-based distributor has recalled over 19,000 cases of Dr. Pepper Zero Sugar due to a labeling error that led to full-sugar products being packaged as sugar-free. The recall, classified as Class II by the FDA, affects products distributed in Florida, Georgia, and South Carolina. Consumers are advised to check packaging for a best-by date of February 16, 2026, and should not consume the affected products. No adverse health effects have been reported, but the situation emphasizes the importance of accurate labeling.

Jacksonville

The Jacksonville-based Pepsi distributor has announced a recall of over 19,000 cases of Dr. Pepper Zero Sugar, due to a labeling error that resulted in the packaging containing full sugar beverages instead of the intended sugar-free versions. This recall was officially initiated on May 23, 2025, and remains ongoing.

According to the Food and Drug Administration (FDA), a total of 19,203 cases have been affected by this mix-up. The mislabeling issue concerns 12 FL OZ (355 mL) aluminum cans which were packaged in both 12-pack and 24-pack cartons. These products were distributed to various retail locations across Florida, Georgia, and South Carolina.

The FDA has classified this recall as a Class II recall, which indicates a low risk of serious health consequences for most consumers. Despite the mislabeling, there have been no reports of illnesses or adverse reactions related to the affected products. However, consumers are strongly advised not to consume, sell, or distribute any of the recalled cases.

Guidance for Consumers

Consumers who may have purchased the recalled Dr. Pepper should check their inventories for the affected product code and best-by date. The recalled products carry a best-by date of February 16, 2026. Individuals are encouraged to look for the specific labeling that misidentifies full-sugar products as Dr. Pepper Zero Sugar.

Production and Distribution Details

The mispackaged products were produced at a Pepsi bottling facility located near the intersection of Bowden Road and I-95 in Jacksonville, Florida. The distribution of these products was extensive, making it critical for consumers in the affected states to be informed about the recall.

Health Considerations

Mislabeled products can present health risks, particularly for consumers with dietary restrictions, such as those managing diabetes. Unexpected consumption of full-sugar beverages can lead to temporary health effects like elevated blood sugar levels or digestive discomfort, making the current recall a matter of consumer safety.

Background on FDA Food and Beverage Recalls

In 2024, the FDA recorded a total of 241 food and beverage recalls, with the majority stemming from undeclared allergens or ingredients. Manufacturers and distributors are required to adhere to strict labeling regulations to ensure that consumers are fully informed about the products they purchase. The FDA is working closely with Dr. Pepper and the involved bottling facilities to ensure that the affected products are swiftly removed from retail shelves.

Popularity of Soft Drinks

Dr. Pepper, alongside Pepsi, was noted as one of the second most popular sodas in the United States the previous year, following Coca-Cola. The widespread distribution and high consumption rates of these beverages emphasize the importance of maintaining accuracy in product labeling.

Consumers are urged to remain vigilant about the products they purchase and to pay attention to any recall announcements that may impact them. As the situation develops, further updates regarding the recall will be communicated through official channels.

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