Class IITerminated in FDA datasetRecall initiated Aug 12, 2022

Capri Sun, Wild Cherry, Flavored Juice Drink Blend in 6floz. foil pouch. Sold in carton…

Recalling firm: KRAFT HEINZ FOODS COMPANY

Why it was recalled

cleaning solution, which is used on food processing equipment, was inadvertently introduced into a production line

Historical recall record. This is not a new recall announcement. “Terminated” describes the FDA recall process; it does not certify that an individual package is safe. FDA termination date: Jun 28, 2023.

Check your package

Compare the exact product and package details with the label you have.

ProductCapri Sun, Wild Cherry, Flavored Juice Drink Blend in 6floz. foil pouch. Sold in carton containing 10 pouches. Carton UPC 087684001004. Four cartons per wholesale case.
Package size6floz
UPC087684001004

FDA code information

The Best When Used By date on the products is June 25, 2023 Carton code: 25JUN2023 WXX #### CT1404 Notes: XX may be 01, 02, or 03 #### would be between 0733-1000 Pouch code: 25JUN2023 WXX LYY #### Notes: XX may be 01, 02, 03, 04, 09, or 10. YY may be 01 through 12 #### would be between 0733-0900

Match the product, package size, and code together. A missing match does not guarantee safety.

Full FDA record and distribution details

Original product description

Capri Sun, Wild Cherry, Flavored Juice Drink Blend in 6floz. foil pouch. Sold in carton containing 10 pouches. Carton UPC 087684001004. Four cartons per wholesale case.

Extracted codes and context

TypeCode / valueContext
UPC087684001004k Blend in 6floz. foil pouch. Sold in carton containing 10 pouches. Carton UPC 087684001004. Four cartons per wholesale case.

Original FDA recall reason

cleaning solution, which is used on food processing equipment, was inadvertently introduced into a production line

Recall details

Recall number
F-1735-2022
Event ID
90744
FDA status
Terminated
Initiated
Aug 12, 2022
Reported
Sep 21, 2022
Classified
Sep 13, 2022
Terminated
Jun 28, 2023
Quantity
5,760 cases
Location
Chicago, IL, United States
Initiation type
Voluntary: Firm initiated
Notification
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit

Where it was distributed

IL, IN, MD, MS,NJ, NY, PA, VA

FDA source record · F-1735-2022

Data updated September 16, 2026. View official FDA data ↗

Follow official FDA and manufacturer guidance.