Zero Sugar Mix-Up On Popular Drink Sparks Massive Recall Across Three States

Clear Facts

• Minute Maid “Zero Sugar” Lemonade was recalled due to mislabeling, as it contained full-sugar lemonade instead.
• The recall affected products distributed in Kentucky, Indiana, and Ohio.
• A total of 13,152 cases were recalled, but no affected products remain on store shelves.

In a recent announcement, the Food and Drug Administration (FDA) revealed that thousands of cases of Minute Maid “Zero Sugar” Lemonade were pulled from the market. The recall was initiated because these cans actually contained the full-sugar version of the lemonade, contrary to what the labels indicated.

This mislabeling issue affected products distributed in three states: Kentucky, Indiana, and Ohio. According to a statement from Coca-Cola, the parent company of Minute Maid, the impacted products have been removed from store shelves, ensuring that consumers in these areas are not at risk of purchasing the mislabeled lemonade.

A Coca-Cola representative confirmed that the company “voluntarily recalled a limited quantity” of the affected 12-ounce cans in the specified states.

“No impacted product remains in the market, and all recall activities in those markets are complete,” the representative assured.

The scale of the recall was significant, with 13,152 cases being affected, as noted in the FDA’s release. Each case contained 12 cartons, with each carton holding 12 cans of lemonade.

The discrepancy between the two products is notable. Minute Maid Zero Sugar, as described on Coca-Cola’s website, is sweetened with aspartame and contains zero grams of sugar. In contrast, the standard Minute Maid Lemonade contains 28 grams of sugar per cup, a substantial difference for those monitoring their sugar intake.

The FDA classified this incident as a “Class II” recall. According to the FDA’s website, a “Class II” recall is defined as a situation where the use of, or exposure to, a violative product may cause temporary or medically reversible adverse health consequences, with the probability of serious adverse health consequences being remote. This classification is less severe than a “Class I” recall, which indicates a high likelihood of causing serious injury or death.

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