KRAFT HEINZ FOODS COMPANY Recall: potential for glass and metal in product - F-0322-2022

🇺🇸 United States

1. November 11, 2021 - Recall initiated
2. December 22, 2021 - Reported by source
3. September 6, 2024 - Recall terminated

Official source record

Agency

FDA

Dataset

FDA Food Enforcement (Recalls)

Recall number

F-0322-2022

Event ID

89053

Status

Terminated

Classification

Class II

Company

KRAFT HEINZ FOODS COMPANY

Product description

Country Time Lemonade drink mix powder 19 oz. UPC 043000951170 29 oz. UPC 043000951194 63 oz. UPC 043000082195 82.5 oz. UPC 043000928608 116 oz. UPC 043000075388

Quantity

289,221 cases (total)

Reason

potential for glass and metal in product

Recall initiation date

November 11, 2021

Report date

December 22, 2021

Classification date

Not published in this source record

Termination date

September 6, 2024

Distribution pattern

Nationwide, Puerto Rico, Guam, American Samoa, Aruba, Saipan, Bermuda, Jamaica, Guyana, South Korea, Canada

UPC, lot, and code information

UPC 043000951170; Best When Used By dates between: 19 oz. 6/20/2023-9/11/2023 29 oz. 8/10/2023 63 oz. 8/8/2023-9/6/2023 82.5 oz. 8/6/2023-10/22/2023 116 oz. 5/10/2023-8/10/2023

Voluntary or mandated

Voluntary: Firm initiated

Initial notification method

Letter

Source last updated

Not tracked separately from the Public Health Trace retrieval date below

Public Health Trace retrieval date

July 18, 2026 ET

Other products recalled under this same event

This recall shares FDA event ID 89053 with 10 other product entries in Public Health Trace.

Responsible company: KRAFT HEINZ FOODS COMPANY

Other recalls from KRAFT HEINZ FOODS COMPANY

Where this information comes from

View FDA enforcement record -- the specific openFDA record this summary was built from.

This record comes from FDA's Enforcement Report database. Not every Enforcement Report record has a separate FDA.gov recall-announcement page.

FDA Enforcement Reports -- FDA's general, official recall and enforcement information. See FDA Enforcement Reports versus recall announcements for how that database differs from a press-release-style announcement.

New to reading a recall record? See how to read an FDA recall record and what recall statuses mean.

Technical source data

View raw source data -- the machine-readable record this page's information was built from.

Retrieved by Public Health Trace: July 18, 2026 ET

Frequently asked questions

What does a Class II mean?

FDA classifies this recall as Class II. See how to read an FDA recall record (linked above) for what each classification level means.

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 responsible agency's published instructions, linked below -- recall guidance is set by that agency, not by Public Health Trace.

Official guidance and record verification

Public Health Trace does not provide medical advice -- review the linked official source below for current, authoritative information.

How to interpret this historical record

This record is preserved as published by FDA, as of September 6, 2024.

Status as reported: Terminated.

This page does not imply a current danger or a current consumer instruction -- review the official source for the most current information.

View the official FDA source

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.

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