Coca Cola Zero, 2 liter pet bottle, UPC 49000 05014, The Coca Cola Company
Coca-Cola Company (The) recalled this product and the FDA reported the enforcement action on 31 December 2014 as Class III. The recall was initiated by the firm. Equipment malfunction led to ingredients to be blended at levels that are inconsistent with approved formulations.
The record
Every field below is published by the FDA in the openFDA food enforcement database. Check the FDA notice before acting on any recall: this page is a reading of the public record, not a substitute for it.
- Product
- Coca Cola Zero, 2 liter pet bottle, UPC 49000 05014, The Coca Cola Company
- UPC
- 4900005014
- Reason for recall
- Equipment malfunction led to ingredients to be blended at levels that are inconsistent with approved formulations.
- Recalling firm
- Coca-Cola Company (The)
- Firm location
- Atlanta, Georgia, United States
- Classification
- Class III
- Status
- Terminated
- Recall number
- F-0754-2015
- Quantity
- 600 bottles (75 cases)
- Distribution
- OH, KY and IN.
- Initiated
- 5 November 2014
- Reported by FDA
- 31 December 2014
- Terminated
- 27 July 2015
- Firm notified by
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
- Product codes
- Date code: DEC1514 CNB, Time Stamps: 12:19, 12:20, 12:21 and 12:22
Reading this record
Five things about this record are not in the record itself, and each one changes how it should be read.
- Class III means the FDA judged that the product was unlikely to cause harm but violated FDA labelling or manufacturing regulation. The class is assigned by an agency health hazard evaluation under 21 CFR 7.41, not by the firm.
- The firm started this recall itself. Most FDA food recalls are voluntary, and a recall is a food safety plan working rather than failing. The circumstances in which the agency asks for one instead are set out in 21 CFR 7.45.
- This record is the only one the FDA opened for its recall event, so it covers a single product code.
- The recall ran for 9 months, from 5 November 2014 to termination on 27 July 2015. Termination means the agency judged that all reasonable effort had been made, under 21 CFR 7.55, and it says nothing about whether product remained in circulation.
- The distribution pattern names 3 states, and the FDA published the enforcement report 8 weeks after the firm began the recall.
- The product description on this record names no food this site can classify, so it appears on no food-type page. That is a limit of the description rather than of the recall.
Named in the distribution pattern: Ohio, Kentucky, Indiana. Those pages count recalls by where the RECALLING FIRM sits, which is a different question from where this product went.
Other records from Coca-Cola Company (The)
The FDA opens one enforcement record per product code, so several of these are frequently one recall event. 13 other records name this firm.
All 14 records for Coca-Cola Company (The)
All 2014 recalls · All FDA food recall data
Behind every recall is a clause somebody has to produce evidence for at their next audit. Krolda maps supplier documents to the clause they satisfy in FSSC 22000, IFS Food and 21 CFR 117, and routes the corrective action when the evidence is missing.
Early accessRecall records come from the openFDA food enforcement API, published by the U.S. Food and Drug Administration in the public domain. Krolda adds the hazard classification and the clause mapping; neither is an FDA determination. Always check the FDA notice before acting on a recall.