RANDALL GREAT NORTHERN BEANS 48OZ glass jar UPC 070095000100; RANDALL GREAT NORTHERN BEANS 24OZ glass jar UPC 0700950001
Summary
The FDA issued a Class II for RANDALL GREAT NORTHERN BEANS 48OZ glass jar UPC 070095000100; RANDALL GREAT NORT by Randall Foods, Inc.. Reason: Lack of functioning Temperature Indicating Devices in retorts.
Details
Source
Food Recall
External ID
F-0798-2021
Action Date
2021-08-04
Status
Terminated
Category
food
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
Lot/Code Info: Randall products: All lots All Best By dates Prior to January 1 2025 Hurst's product: Lot TGN19253 Best By date 9/9/2022
Quantity Affected: 800,000 cases (total)
Reason for Recall
Lack of functioning Temperature Indicating Devices in retorts
Distribution
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.
Type: Voluntary: Firm initiated
Recall Initiated: 2021-05-19
Company
Tekonsha, MI
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 31 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Randall Foods, Inc. has 8 FDA actions in our database, including 8 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 (Randall Foods, Inc.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Randall Foods, Inc. have FDA actions?
Randall Foods, Inc. has 8 FDA actions in our database, including 8 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-0798-2021" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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