FDA recall record
Diet Coke, 12 oz (355 mL) cans, packed in 12 and 24 packs, Canned under the authority of the Coca-Cola Company, Atlanta, GA
FDA classification. FDA Class I, II, and III are not the same as USDA FSIS classifications and are not a cross-agency safety score.
FDA listed a termination date of July 5, 2018. openFDA does not treat this as a live recall-status tracker.
Product described in an FDA recall
Diet Coke, 12 oz (355 mL) cans, packed in 12 and 24 packs, Canned under the authority of the Coca-Cola Company, Atlanta, GA
Reason
Sharp edges were observed on several of the cans which have the potential of causing cuts on the mouths of consumers who use the product.
Products involved
Product descriptions are copied from the FDA recall record. They are not a current catalog and are not automatically matched to WhoMadeMyFood product pages.
Diet Coke, 12 oz (355 mL) cans, packed in 12 and 24 packs, Canned under the authority of the Coca-Cola Company, Atlanta, GA
Code information listed by FDA
12 packs: Mar 19 18 LXE, Apr 09 18 LXE, Apr 02 18 LXC; 24 packs: Mar 19 18 LXE, Mar 26 18 LXB, Mar 26 18 LXC, Apr 02 18 LXE, Apr 09 18 LXA, Apr 09 18 LXE, Apr 16 18 LXC
Distribution and firm information
Recalling firm listed by FDA: Heartland Coca-Cola Bottling Company
Firm location listed by FDA: Lenexa, KS, United States
Distribution reported by FDA: Distributed to retail stores in AR, IA, IL, KS, MO, and NE.
Product quantity listed by FDA: 766,271 Cases Total
Source
Source: U.S. Food and Drug Administration (FDA), openFDA food enforcement reports.
Official FDA openFDA food enforcement record
Identifying an FDA recall record does not imply FDA endorsement of WhoMadeMyFood. Methodology.