RecallHawk
Class II Recall

Arizona Arnold Palmer Half Iced Tea & Half Lemonade drink mix powder 73 oz. UPC 043000086643

KRAFT HEINZ FOODS COMPANY

Summary

The FDA issued a Class II for Arizona Arnold Palmer Half Iced Tea & Half Lemonade drink mix powder 73 oz. UP by KRAFT HEINZ FOODS COMPANY. Reason: potential for glass and metal in product.

Details

Source

Food Recall

External ID

F-0326-2022

Action Date

2021-12-22

Status

Terminated

Category

food

Product Description

Arizona Arnold Palmer Half Iced Tea & Half Lemonade drink mix powder 73 oz. UPC 043000086643

Lot/Code Info: Best When Used By dates between: 8/5/2023-9/10/2023

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

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-0326-2022" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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