Farmers' All Natural Creamery LLC Recall: Milk products and shipped without being properly pasteurized.

🇺🇸 United States

1. September 17, 2021 - Recall initiated
2. October 27, 2021 - Reported by source
3. November 1, 2021 - Recall terminated

Official source record

Agency

FDA

Dataset

FDA Food Enforcement (Recalls)

Recall number

F-0020-2022

Event ID

88745

Status

Terminated

Classification

Class II

Company

Farmers' All Natural Creamery LLC

Product description

Kalona Supernatural Organic Whipping Cream, Manufactured in Iowa for Kalona Organics, LLC. Kalona IA in 16 FL OZ (UPC 8-81245-12016-2, 8 bottles per case) and 32 FL OZ (UPC 8-81245-12032-2, 6 bottles per case)

Quantity

253 cases of 16 OZ, 325 cases of 32 OZ

Reason

Milk products and shipped without being properly pasteurized.

Recall initiation date

September 17, 2021

Report date

October 27, 2021

Classification date

Not published in this source record

Termination date

November 1, 2021

Distribution pattern

Distributed to retail food store distributors in CA, CO, IA, IL, MN, TX, and WI

UPC, lot, and code information

UPC 8-81245-12016-2; 10/6/21

Voluntary or mandated

Voluntary: Firm initiated

Initial notification method

Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit

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 88745 with 2 other product entries in Public Health Trace.

Responsible company: Farmers' All Natural Creamery LLC

Other recalls from Farmers' All Natural Creamery 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
California	1
Colorado	1
Iowa	1
Illinois	1
Minnesota	1
Texas	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.

No separate FDA public notice was found for this enforcement record. The information below comes from FDA's Recall Enterprise System through openFDA.

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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