Heinz Real Vraie Mayonnaise
Reason undeclared ingredients including but not limited to mustard
Capri Sun Wild Cherry recall
Recalled by Kraft Heinz Foods Company · Chicago, IL, United States
Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.
Why it was recalled
cleaning solution, which is used on food processing equipment, was inadvertently introduced into a production line
These are failures of the safety steps that keep food safe - cooking, pasteurising, keeping cold, sealing - even when no contaminant has yet been found. All processing & sanitation problems recalls.
What was recalled
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
Food: Juice & beverages
Lot codes, dates and UPCs
A recall covers only these codes. Compare them with the lot number, best-by date or UPC printed on your package.
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
Where it was sold
Illinois Indiana Maryland Mississippi New Jersey New York Pennsylvania Virginia
FDA's distribution note: IL, IN, MD, MS,NJ, NY, PA, VA
Check the codes, then return or discard. Class II means eating it may cause temporary or reversible health problems. If your package matches the recalled codes, do not eat it - return it to the store or throw it away. FDA lists this recall as terminated: the company has finished removing the product, so it should no longer be on shelves - but it can still be in a freezer or pantry.
- Recalling firm
- Kraft Heinz Foods Company
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Aug 12, 2022
- In FDA report of
- Sep 21, 2022
- Terminated
- Jun 28, 2023
- FDA recall number
- F-1735-2022 · event 90744
- Official record
- FDA enforcement report search
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