Coca-Cola (Coca-Cola Company) – Can Defect (2016)
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, 16 fl. oz. can/12 pack, UPC 049000054318; Coca-Cola, 12 oz. can/12 pack, UPC 049000028904; Coca-Cola Zero, 12 oz. can/12 pack, UPC 049000042559; Diet Coke, 12 oz. can/24 pack, UPC 049000010633; Diet Coke, 12 oz. can/12 pack, UPC 049000028911; Cherry Coke, 12 oz. can/12 pack, UPC 049000031034
Brand
Coca-Cola Company (The)
Lot Codes / Batch Numbers
Date Code/Lot Code - UPC 049000053418 - JAN0217 VJ E, UPC 049000028904 - JAN0917TRE, UPC 049000042559 - AUG1516TRD, UPC 049000010633 - JUL1116TRE, UPC 049000028911 - JUL1116TRB, UPC049000031034 - JAN0917TRD
Products Sold
Date Code/Lot Code - UPC 049000053418 - JAN0217 VJ E; UPC 049000028904 - JAN0917TRE; UPC 049000042559 - AUG1516TRD; UPC 049000010633 - JUL1116TRE; UPC 049000028911 - JUL1116TRB; UPC049000031034 - JAN0917TRD
Coca-Cola Company (The) is recalling Coca-Cola, 16 fl. oz. can/12 pack, UPC 049000054318; Coca-Cola, 12 oz. can/12 pack, UPC 049000028904 due to In a small percentage of the cans, when opened, the oval covering for the hole, which normally is pushed down into the can, instead opens upward. Thi. 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
In a small percentage of the cans, when opened, the oval covering for the hole, which normally is pushed down into the can, instead opens upward. This produces a loud "pop" sound. Recall initiated on 4/29/16.
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
AZ, OR, WA
Page updated: Jan 6, 2026