Capri Sun, Wild Cherry, Flavored Juice Drink Blend in 6floz. foil pouch. Sold in carton containing 10 pouches. Carton U
Summary
The FDA issued a Class II for Capri Sun, Wild Cherry, Flavored Juice Drink Blend in 6floz. foil pouch. Sold in by KRAFT HEINZ FOODS COMPANY. Reason: cleaning solution, which is used on food processing equipment, was inadvertently introduced into a production line.
Details
Source
Food Recall
External ID
F-1735-2022
Action Date
2022-09-21
Status
Terminated
Category
food
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.
Lot/Code Info: 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
Quantity Affected: 5,760 cases
Reason for Recall
cleaning solution, which is used on food processing equipment, was inadvertently introduced into a production line
Distribution
IL, IN, MD, MS,NJ, NY, PA, VA
Type: Voluntary: Firm initiated
Recall Initiated: 2022-08-12
Company
Chicago, IL
Context & Analysis
This is a Class II recall. Class II recalls indicate that use of or exposure to the product may cause temporary or medically reversible health consequences, or that the probability of serious consequences is remote.
This was one of 49 food recalls issued in the same week, part of 204 food-related FDA actions this month.
KRAFT HEINZ FOODS COMPANY has 16 FDA actions in our database, including 16 recalls.
Frequently Asked Questions
What is a Class II recall?
A Class II recall means the product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse consequences is remote. Consumers should discontinue use.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (KRAFT HEINZ FOODS COMPANY) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does KRAFT HEINZ FOODS COMPANY have FDA actions?
KRAFT HEINZ FOODS COMPANY has 16 FDA actions in our database, including 16 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-1735-2022" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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