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Policy version 2026-07-21, effective July 21, 2026.
United States
TerminatedClass II
cleaning solution, which is used on food processing equipment, was inadvertently introduced into a production line
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| 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. | 087684001004 | 5,760 cases | 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 |
Responsible company: KRAFT HEINZ FOODS COMPANY
FDA Recall United States TerminatedTerminated: January 21, 2025Historical recordClass II
FDA Recall United States TerminatedTerminated: September 6, 2024Historical recordClass II
FDA Recall United States TerminatedTerminated: September 6, 2024Historical recordClass II
A map highlighting the states named in the source's distribution description.
Shading reflects state-level totals only, as published by the source. It does not imply county-level or point-level precision.
| State | Distributed |
|---|---|
| Illinois | 1 |
| Indiana | 1 |
| Maryland | 1 |
| Mississippi | 1 |
| New Jersey | 1 |
| New York | 1 |
| Pennsylvania | 1 |
| Virginia | 1 |
States shown are extracted from the source's free-text distribution description above; a narrative description (e.g. "distributed nationwide") may not list individual states to extract.
View FDA enforcement record -- the specific openFDA record this summary was built from.
This record comes from FDA's Enforcement Report database. Not every Enforcement Report record has a separate FDA.gov recall-announcement page.
FDA Enforcement Reports -- FDA's general, official recall and enforcement information.
View raw source data -- the machine-readable record this page's information was built from.
Retrieved by Public Health Trace:
A situation in which use of or exposure to a product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote.
According to FDA, this recall's status is "Terminated." Always confirm the current status using the source links below, since status can change after Public Health Trace last retrieved this record.
Follow the instructions published by the responsible agency (see the source links below) -- recall guidance (e.g. dispose of the product, return it for a refund, or check for a specific lot number) varies by recall and is set by that agency, not by Public Health Trace.
The source links below, published by FDA, are the authoritative record for this recall, including any updates issued after this summary was retrieved.
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This record is preserved as published by FDA, as of June 28, 2023.
Status as reported: Terminated.
This page does not imply a current danger or a current consumer instruction -- review the official source for the most current information.
This summary is based on the official source record referenced above. Public Health Trace does not state that any company or product is unsafe beyond what the official source has published. Read the full medical disclaimer.
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