FDA recall record

Coca-Cola Company Coca Cola Zero, 2 liter pet bottle, UPC 49000 05014, The Coca recall — FDA F-0754-2015

Equipment malfunction led to ingredients to be blended at levels that are inconsistent with approved formulations.

Class IIIclassification
F-0754-2015official record ID
Dec 31, 2014report date

Recall record at a glance

Official recordF-0754-2015
CategoryFood Recalls
ClassificationClass III
FDA record statusTerminated
Recalling firmCoca-Cola Company (The)
Report dateDec 31, 2014
Recall initiation dateNov 5, 2014
Quantity600 bottles (75 cases)
LocationAtlanta, GA, United States

Official product description

Coca Cola Zero, 2 liter pet bottle, UPC 49000 05014, The Coca Cola Company

Why the product was recalled

Equipment malfunction led to ingredients to be blended at levels that are inconsistent with approved formulations.

Distribution information

OH, KY and IN.

How to read the classification

FDA Class III generally covers situations in which use of or exposure to the product is not likely to cause adverse health consequences. The classification displayed here is taken from the FDA enforcement record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

Recall Lookup USA preserves the most complete source information successfully retrieved. We do not create missing facts or infer affected lots or VINs. The official record may still change, so use the identifier above when verifying current instructions.

FDA source limitation: openFDA enforcement reports are a reference dataset, not a live public-alert or recall-lifecycle service. FDA notes that enforcement-report status may not be updated after classification. Confirm current actions with the FDA, recalling firm or appropriate healthcare professional when relevant.

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