Coca-Cola Original (Heartland Coca-Cola) – Sharp Can Edges (2018)
Class II: A situation in which use of, or exposure to, a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote
Class II recall indicates potential for temporary health effects.
This AI-generated summary is provided for general informational purposes only and is derived from publicly available recall notices. It supplements but does not replace official agency classifications or safety instructions.
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Coca-Cola, Original Taste, 12 oz (355 mL) cans, packed in 12 and 24 packs, Canned under the authority of the Coca-Cola Company, Atlanta, GA
Brand
Heartland Coca-Cola Bottling Company
Lot Codes / Batch Numbers
12 packs: Sep 17 18 LXF, Oct 01 18 LXC, Oct 01 18 LXF, Oct 08 18 LXC, Oct 15 18 LXD, Oct 15 18 LXE, Oct 22 18 LXB, Sep 24 18 LXC, 24 packs: Sep 17 18 LXE, Sep 24 18 LXB, Sep 24 18 LXC, Oct 01 18 LXC, Oct 08 18 LXB, Oct 08 18 LXE
Products Sold
12 packs: Sep 17 18 LXF, Oct 01 18 LXC, Oct 01 18 LXF, Oct 08 18 LXC, Oct 15 18 LXD, Oct 15 18 LXE, Oct 22 18 LXB, Sep 24 18 LXC; 24 packs: Sep 17 18 LXE, Sep 24 18 LXB, Sep 24 18 LXC, Oct 01 18 LXC, Oct 08 18 LXB, Oct 08 18 LXE
Heartland Coca-Cola Bottling Company is recalling Coca-Cola, Original Taste, 12 oz (355 mL) cans, packed in 12 and 24 packs, Canned under the authorit due to 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.. This is a Class I recall, indicating a high risk of serious health consequences. Based on FDA enforcement report.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
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.
Recommended Action
Per FDA guidance
Consumers should stop using the product and contact the recalling firm or return it to the place of purchase.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticeDistribution
As reported by FDA
AR, IL, IN, IA, KS, MO, NE
Page updated: Jan 6, 2026