FDA Recall United States Terminated Historical recordClass II
KRAFT HEINZ FOODS COMPANY
- Product
- Primal Kitchen Avocado Oil 1PT 9.3 FL OZ (750ml) glass bottl…
- Published
- July 24, 2024
- Distribution
- ME, CA, GA, IN, KY, NC, NV, PA, AZ, TX a…
KRAFT HEINZ FOODS COMPANY Recall: cleaning solution, which is used on food processing equipment, was inadvertently introduced into a production line
United States
TerminatedClass II
- Company
- KRAFT HEINZ FOODS COMPANY
- Product
- Capri Sun, Wild Cherry, Flavored Juice Drink Blend in 6floz.…
- Recall date
- August 12, 2022
- Terminated
- June 28, 2023
- Source
- FDA
Reason for recall
cleaning solution, which is used on food processing equipment, was inadvertently introduced into a production line
- - Recall initiated
- - Reported by source
- - Recall terminated
| 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 |
Distribution
- IL
- IN
- MD
- MS
- NJ
- NY
- PA
- VA
Official source record
- Agency
- FDA
- Dataset
- FDA Food Enforcement (Recalls)
- Recall number
- F-1735-2022
- Event ID
- 90744
- Status
- Terminated
- Classification
- Class II
- Company
- KRAFT HEINZ FOODS COMPANY
- 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.
- Quantity
- 5,760 cases
- Reason
- cleaning solution, which is used on food processing equipment, was inadvertently introduced into a production line
- Recall initiation date
- August 12, 2022
- Report date
- September 21, 2022
- Classification date
- Not published in this source record
- Termination date
- June 28, 2023
- Distribution pattern
- IL, IN, MD, MS,NJ, NY, PA, VA
- UPC, lot, and code information
- UPC 087684001004; 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
- Voluntary or mandated
- Voluntary: Firm initiated
- Initial notification method
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
- Source last updated
- Not tracked separately from the Public Health Trace retrieval date below
- Public Health Trace retrieval date
Responsible company: KRAFT HEINZ FOODS COMPANY
Other recalls from KRAFT HEINZ FOODS COMPANY
FDA Recall United States Terminated Historical recordClass II
KRAFT HEINZ FOODS COMPANY
- Product
- Tang guava pineapple drink mix powder 18 oz. UPC 043000064…
- Published
- December 22, 2021
- Distribution
- Nationwide
FDA Recall United States Terminated Historical recordClass II
KRAFT HEINZ FOODS COMPANY
- Product
- Tang orange drink mix powder 20 oz. UPC 043000032275 58.9…
- Published
- December 22, 2021
- Distribution
- Nationwide
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.
Where this information comes from
View FDA enforcement record -- the specific openFDA record this summary was built from.
No separate FDA public notice was found for this enforcement record. The information below comes from FDA's Recall Enterprise System through openFDA.
FDA Enforcement Reports -- FDA's general, official recall and enforcement information.
Technical source data
View raw source data -- the machine-readable record this page's information was built from.
Retrieved by Public Health Trace:
Frequently asked questions
What does a Class II mean?
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.
Is this recall still active?
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.
What should I do if I have this product?
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.
Where can I find more official information?
The source links below, published by FDA, are the authoritative record for this recall, including any updates issued after this summary was retrieved.
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.
