Kool-Aid strawberry drink mix powder 19 oz. UPC 043000953556
Summary
The FDA issued a Class II for Kool-Aid strawberry drink mix powder 19 oz. UPC 043000953556 by KRAFT HEINZ FOODS COMPANY. Reason: potential for glass and metal in product.
Details
Source
Food Recall
External ID
F-0329-2022
Action Date
2021-12-22
Status
Terminated
Category
food
Product Description
Kool-Aid strawberry drink mix powder 19 oz. UPC 043000953556
Lot/Code Info: Best When Used By dates between: 10/18/2023-10/19/2023
Quantity Affected: 289,221 cases (total)
Reason for Recall
potential for glass and metal in product
Distribution
Nationwide, Puerto Rico, Guam, American Samoa, Aruba, Saipan, Bermuda, Jamaica, Guyana, South Korea, Canada
Type: Voluntary: Firm initiated
Recall Initiated: 2021-11-11
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 42 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-0329-2022" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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