Honeyville YELLOW COLOR
Reason Undeclared Red #40.
DASANI Purified Water recall
Recalled by World of Coca-Cola · Atlanta, GA, United States
Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.
Why it was recalled
There is the potential that some of the bottles may contain linear pieces of plastic from the bottle production.
Hard or sharp fragments can cut the mouth or throat, break teeth or cause choking. They usually come from equipment wear or packaging on the production line. All foreign material recalls.
What was recalled
DASANI Purified Water, 24/20 fl. oz. (1.25 pt) 591 mL, pack, Desani, The Coca Cola Company, Atlanta, GA 30313.
Quantity: 328,337 cases (24 bottlers per case)
Food: Juice & beverages
Lot codes, dates and UPCs
A recall covers only these codes. Compare them with the lot number, best-by date or UPC printed on your package.
UPC Code: 0 499770 4, Date Codes: MAR 2116 KMA, MAR 2116 KMB, MAR 2116 KMC, MAR 2116 KMD, MAR 2816 KM A, MAR 2816 KM B, MAR 2816 KM C, MAR 2816 KM D, MAR 2816 KM E, MAR 2816 KM F, APR 1116 KM A, APR 1116 KM B, APR 1116 KM D, APR 1116 KM E, APR 1816 KM A, APR 1816 KM B, APR 1816 KM C, APR 1816 KM D, APR 1816 KM E and APR 2516 KM B.
Where it was sold
Connecticut District of Columbia Delaware Massachusetts Maryland North Carolina New Hampshire New Jersey New York Pennsylvania Rhode Island Virginia Vermont West Virginia
FDA's distribution note: CT, DC, DE, MA, MD, NC, NH, NJ, NY, PA, RI, VA, VT and WV.
Check the codes, then return or discard. Class II means eating it may cause temporary or reversible health problems. If your package matches the recalled codes, do not eat it - return it to the store or throw it away. FDA lists this recall as terminated: the company has finished removing the product, so it should no longer be on shelves - but it can still be in a freezer or pantry.
- Recalling firm
- World of Coca-Cola
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- May 8, 2015
- In FDA report of
- Jul 15, 2015
- Terminated
- Apr 7, 2016
- FDA recall number
- F-2789-2015 · event 71286
- Official record
- FDA enforcement report search
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