Minute Maid Strawberry Passion Juice (Coca-Cola) – potential bottle issue (2013)
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
MINUTE MAID STRAWBERRY PASSION Flavored Juice Beverage, 15.2 oz plastic (PET) bottles, Produced for The Coca Cola Company, Atlanta, GA 30313 USA.
Brand
Coca-Cola Refreshments USA, Inc.
Lot Codes / Batch Numbers
Optimum Taste Date Code: NOV0413MDD3 and NOV1113MDA3, UPC Code: 025000048906.
Products Sold
Optimum Taste Date Code: NOV0413MDD3 and NOV1113MDA3, UPC Code: 025000048906.
Coca-Cola Refreshments USA, Inc. is recalling MINUTE MAID STRAWBERRY PASSION Flavored Juice Beverage, 15.2 oz plastic (PET) bottles, Produced for due to Products with the specific Lot Code and UPC Codes listed above are being retrieved because there is the potential that some of the bottles could exhib. 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
Products with the specific Lot Code and UPC Codes listed above are being retrieved because there is the potential that some of the bottles could exhibit spoilage or damage to the lip of the bottle.
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 noticePage updated: Jan 6, 2026