Coca-Cola recalls Minute Maid 'Zero Sugar' Lemonade due to mislabeling

Coca-Cola recalls Minute Maid ‘Zero Sugar’ Lemonade due to mislabeling

Thousands of cases of Minute Maid “Zero Sugar” Lemonade that actually contained the standard, full-sugar lemonade were recalled in September, the Food and Drug Administration announced. 

The mislabeled cans of lemonade were sent to stores in three states — Kentucky, Indiana and Ohio, the FDA said.

A statement from Coca-Cola, which owns Minute Maid, said that the impacted items were no longer on store shelves and customers in these states should not be concerned they were drinking a mislabeled product. 

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A representative from Coca-Cola told Fox News Digital in an email on Wednesday that the company “voluntarily recalled a limited quantity” of the 12-ounce cans in the three states noted. 

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

Labels applied to bottles of Minute Maid lemonade.

The recalled Minute Maid Zero Sugar Lemonade cans contained the standard Minute Maid Lemonade, seen here in bottle form.  (George Frey/Getty Images)

A total of 13,152 cases of the mislabeled lemonade were recalled, according to the FDA’s release. 

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Each case contains 12 cartons of 12 cans of lemonade.

FDA sign outside headquarters.

The FDA announced the recall in mid-October after the items were removed from shelves.  (REUTERS/Andrew Kelly/File Photo)

Minute Maid Zero Sugar, which is sweetened with aspartame, has zero grams of sugar, Coca-Cola’s website states.

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Conversely, Minute Maid Lemonade contains 28 grams of sugar per cup. 

The FDA classified the incident as a “Class II” recall on Oct. 10.

Bottles of minute maid in a factory.

Minute Maid Lemonade contains real sugar – 28 grams per cup.  (George Frey/Getty Images)

A “Class II” recall is defined as “a situation in which use of, or exposure to, a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote,” according to the FDA’s website.

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It is less severe than a “Class I” recall, which means there is a “high likelihood” that the impacted product could cause serious injury or death. 

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