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High RiskFDAfda-F-0561-2017UNDECLARED ALLERGEN

Dr. Pepper Cherry, 12oz (12 pack cans), Manufactured under the authority of Doctor Pepper Company, 5301 Legacy Drive, Plano, TX.

Category
Units Affected
1,020
Recall Date
March 31, 2016
Issuing Agency
Hazard
Undeclared Allergen

FDA Recall Notice

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-0561-2017.

The product contains undeclared High-fructose Corn Syrup (HFCS).

Corrective Action (per FDA)

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-0561-2017.

Recall terminated by FDA.

✅ What you should do

  1. Stop using the product if you own it.
  2. Check the model number, lot code, or sell-by date against the recall notice above.
  3. Contact The Coca-cola Company or the retailer where you bought it for a refund, replacement, or repair.
  4. For the most current official instructions, visit the FDA recall page.
  5. If you've been hurt by this product, report the incident to FDA.

Consumer Contact (per FDA)

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-0561-2017.

The Coca-Cola Company

FDA

About the U.S. Food and Drug Administration

The FDA regulates drugs, medical devices, food, cosmetics, and tobacco. Adverse event reports and recall notices are the main public safety signal.

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📣 Report a food, supplement, or cosmetic problem to the FDA

If you had a reaction, found contamination, or experienced a labeling problem with this product, report it to the FDA. The agency uses consumer reports to track emerging safety signals and trigger recalls.

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The Coca-cola Company Recall FAQ

The Coca-cola Company is the subject of a food safety report: Dr. Pepper Cherry, 12oz (12 pack cans), Manufactured under the authority of Doctor Pepper Company, 5301 Legacy Drive, Plano, TX.. The notice was published on March 31, 2016 by the U.S. Food and Drug Administration (FDA). Approximately 1,020 units are potentially affected.