Class IITerminated in FDA datasetRecall initiated May 8, 2015

DASANI Purified Water, 24/20 fl. oz. (1.25 pt) 591 mL, pack, Desani, The Coca Cola Company,…

Recalling firm: World of Coca-Cola

Why it was recalled

There is the potential that some of the bottles may contain linear pieces of plastic from the bottle production.

Historical recall record. This is not a new recall announcement. “Terminated” describes the FDA recall process; it does not certify that an individual package is safe. FDA termination date: Apr 7, 2016.

Check your package

Compare the exact product and package details with the label you have.

ProductDASANI Purified Water, 24/20 fl. oz. (1.25 pt) 591 mL, pack, Desani, The Coca Cola Company, Atlanta, GA 30313.
Package size20 fl. oz

FDA code information

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.

Match the product, package size, and code together. A missing match does not guarantee safety.

Full FDA record and distribution details

Original product description

DASANI Purified Water, 24/20 fl. oz. (1.25 pt) 591 mL, pack, Desani, The Coca Cola Company, Atlanta, GA 30313.

Original FDA recall reason

There is the potential that some of the bottles may contain linear pieces of plastic from the bottle production.

Recall details

Recall number
F-2789-2015
Event ID
71286
FDA status
Terminated
Initiated
May 8, 2015
Reported
Jul 15, 2015
Classified
Jul 7, 2015
Terminated
Apr 7, 2016
Quantity
328,337 cases (24 bottlers per case)
Location
Atlanta, GA, United States
Initiation type
Voluntary: Firm initiated
Notification
Telephone

Where it was distributed

CT, DC, DE, MA, MD, NC, NH, NJ, NY, PA, RI, VA, VT and WV.

FDA source record · F-2789-2015

Data updated September 16, 2026. View official FDA data ↗

Follow official FDA and manufacturer guidance.