Food, drugs, devices › The Coca-Cola Company
Food recall: Honest Kids Juice Slushy Blueberry Punch, 3.5-oz. pouch, UPC 0065762211116.
FDA enforcement event 78041 is a food recall by The Coca-Cola Company of Atlanta, GA, initiated 16 Aug 2017 and classified Class II, with 1 product record.
FDA defines Class II as 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. 52% of the 599 food enforcement events initiated in 2017 carry the same class.
Status: Terminated, terminated 21 Dec 2017. Initiation: voluntary: firm initiated. The Coca-Cola Company has 10 enforcement events on this register, with a median of 1 product record per event.
Recall classification reflects the relative degree of health hazard. Text in quotation marks is FDA's. openFDA export dated 28 Sep 2026.
Recalling firm
The Coca-Cola Company, Atlanta, GA.
Reason for recall
"Due to a potential package design issue, there is the possibility for consumers to be injured when consuming the product from an unevenly opened pouch."
Distribution
"AR, AZ, CA, CO, GA, FL IL, IN, MD, MI, MN, MO, MS, NC, NH, OH, PA, TX and WA."
Product records
| Recall number | Product | Quantity | Class | Status | Report date |
|---|---|---|---|---|---|
| F-3561-2017 | Honest Kids Juice Slushy Blueberry Punch, 3.5-oz. pouch, UPC 0065762211116. | 78,000 cases (18-pack case) | Class II | Terminated | 27 Sep 2017 |
Context
Other enforcement events for The Coca-Cola Company
All 10 events for The Coca-Cola Company
Questions and answers
Why was this food recalled?
FDA's record gives the reason for recall as: "Due to a potential package design issue, there is the possibility for consumers to be injured when consuming the product from an unevenly opened pouch."
What does Class II mean?
FDA classifies recalls by relative degree of health hazard. Class II is 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.
Where was the product distributed?
FDA's distribution pattern field reads: "AR, AZ, CA, CO, GA, FL IL, IN, MD, MI, MN, MO, MS, NC, NH, OH, PA, TX and WA."
Is the recall still ongoing?
FDA lists the status as Terminated; the termination date is 21 Dec 2017. "Terminated" means FDA has determined that all reasonable efforts to remove or correct the product have been made.
Where does this data come from?
openFDA enforcement reports (food, drug and device), CC0, export dated 28 Sep 2026. Text in quotation marks is FDA's. The FDA enforcement report linked above is authoritative.
Provenance
Source: openFDA food enforcement reports (CC0), export dated 28 Sep 2026; records grouped by FDA event number. The class shown for the event is the most severe class among its records. Errors in processing are corrected at the next build; see corrections.