Horizon Organic Dairy, LLC Recall: Potential for premature product spoilage during shelf life.

🇺🇸 United States

1. September 26, 2024 - Recall initiated
2. October 30, 2024 - Reported by source
3. March 17, 2025 - Recall terminated

Official source record

Agency

FDA

Dataset

FDA Food Enforcement (Recalls)

Recall number

F-0064-2025

Event ID

95478

Status

Terminated

Classification

Class II

Company

Horizon Organic Dairy, LLC

Product description

Horizon Organic Ultra Pasteurized Heavy Whipping Cream, refrigerated, One Pint (473ml), UPC 7 42365 21685 5. There are 12 cartons per case. Distributed by: Horizon Organic Dairy, LLC (Horizon) Broomfield, CO 80021.UPC: 742365216855

Quantity

2,956 cases (35,472 units)

Reason

Potential for premature product spoilage during shelf life.

Recall initiation date

September 26, 2024

Report date

October 30, 2024

Classification date

Not published in this source record

Termination date

March 17, 2025

Distribution pattern

Distributed in CT, GA, IN, MD, MA, MD, ME, MI, MO, NY, NC, OK, PA, VA, and WI.

UPC, lot, and code information

UPC 742365216855; BEST BY 10 22 24

Voluntary or mandated

Voluntary: Firm initiated

Initial notification method

E-Mail

Source last updated

Not tracked separately from the Public Health Trace retrieval date below

Public Health Trace retrieval date

July 18, 2026 ET

Responsible company: Horizon Organic Dairy, LLC

Other recalls from Horizon Organic Dairy, LLC

A map highlighting the states named in the source's distribution description.

Distributed No data published

Shading reflects state-level totals only, as published by the source. It does not imply county-level or point-level precision.

Distribution map

State	Distributed
Connecticut	1
Georgia	1
Indiana	1
Maryland	1
Massachusetts	1
Maine	1
Michigan	1
Missouri	1
New York	1
North Carolina	1
Oklahoma	1
Pennsylvania	1
Virginia	1
Wisconsin	1

States shown are extracted from the source's free-text distribution description above; a narrative description (e.g. "distributed nationwide") may not list individual states to extract.

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.

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?

A situation in which use of or exposure to a product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote.

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 instructions published by the responsible agency (see the source links below) -- recall guidance (e.g. dispose of the product, return it for a refund, or check for a specific lot number) varies by recall and is set by that agency, not by Public Health Trace.

Where can I find more official information?

The source links below, published by FDA, are the authoritative record for this recall, including any updates issued after this summary was retrieved.

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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