The U.S. Food and Drug Administration has classified a recall of more than 122,000 cases of Gatorade products. The action addresses beverages that contain food dyes not listed on their labels. PepsiCo initiated the voluntary recall, and the FDA assigned it a Class II designation. Consumers nationwide should verify whether items in their possession match the affected descriptions.
Products and Distribution Details
The recall covers 122,021 cases of 28-ounce bottles in four specific varieties. These include Gatorade Lemon Lime, Gatorade Lemon Lime Zero, Gatorade Orange, and Gatorade Orange Zero. The products contain undeclared Yellow No. 5 and Yellow No. 6 dyes. Distribution reached 37 states. Examples include New York, New Jersey, Pennsylvania, Florida, Texas, and California. The items remain on shelves or in homes until properly identified and removed.
Recall Timeline and Risk Level
PepsiCo began the recall on September 25. The FDA classified it on October 2, and the process continues. A Class II rating indicates that exposure could lead to temporary or reversible health effects, though the chance of serious consequences stays remote. No press release accompanied the enforcement report. Officials instead direct attention to the FDA’s online recall database for full details.
Steps for Consumers
Shoppers should examine lot numbers on any matching Gatorade bottles against the official notice. The FDA provides a direct link to the enforcement report for verification. Returning or disposing of confirmed items follows standard recall procedures. This measure helps maintain accurate labeling across popular beverage lines. Affected households can contact retailers or the manufacturer for further assistance with returns.
AI Disclaimer: This article was created with the assistance of AI tools and reviewed by a human editor.