Randall Foods, Inc. Recall: Lack of functioning Temperature Indicating Devices in retorts

🇺🇸 United States

1. May 19, 2021 - Recall initiated
2. August 4, 2021 - Reported by source
3. February 15, 2022 - Recall terminated

Official source record

Agency

FDA

Dataset

FDA Food Enforcement (Recalls)

Recall number

F-0798-2021

Event ID

88026

Status

Terminated

Classification

Class II

Company

Randall Foods, Inc.

Product description

RANDALL GREAT NORTHERN BEANS 48OZ glass jar UPC 070095000100; RANDALL GREAT NORTHERN BEANS 24OZ glass jar UPC 070095000117; RANDALL GREAT NORTHERN BEANS 15.4OZ glass jar UPC 070095000131; RANDALL ORGANIC GREAT NORTHERN BEANS 48OZ glass jar UPC 070095005105; Hurst's Fully Cooked Great Northern Beans 48OZ glass jar UPC 0 256012 0

Quantity

800,000 cases (total)

Reason

Lack of functioning Temperature Indicating Devices in retorts

Recall initiation date

May 19, 2021

Report date

August 4, 2021

Classification date

Not published in this source record

Termination date

February 15, 2022

Distribution pattern

Retail distribution locations in the following states: Alabama, Arkansas, Florida, Iowa, Illinois, Kansas, Kentucky, Michigan, Minnesota, Missouri, Nebraska, North Carolina, New York, Ohio, Oklahoma, Pennsylvania, South Dakota, Tennessee, Texas, Virginia, Wisconsin, and West Virginia.

UPC, lot, and code information

UPC 070095000100; Randall products: All lots All Best By dates Prior to January 1 2025 Hurst's product: Lot TGN19253 Best By date 9/9/2022

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 88026 with 7 other product entries in Public Health Trace.

Responsible company: Randall Foods, Inc.

Other recalls from Randall Foods, Inc.

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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