Ardent Mills Hotel and Restaurant All Purpose Flour - AA, 50 lb. (22.68kg) bag, UPC 6 78008 00053 9, Ardent Mills, Denve
Summary
The FDA issued a Class II for Ardent Mills Hotel and Restaurant All Purpose Flour - AA, 50 lb. (22.68kg) bag, by Ardent Mills, LLC. Reason: Raw, untreated flour tested positive for Salmonella..
Details
Source
Food Recall
External ID
F-0805-2022
Action Date
2022-03-09
Status
Terminated
Category
food
Product Description
Ardent Mills Hotel and Restaurant All Purpose Flour - AA, 50 lb. (22.68kg) bag, UPC 6 78008 00053 9, Ardent Mills, Denver, CO 80202. Milled in Alton, IL.
Lot/Code Info: Lot: 870749, packaged 11/30/2021, product code: 5162134. Lot: 870749, packaged 12/1/2021, product code: 5162134.
Quantity Affected: 1450 50-lb. bags
Reason for Recall
Raw, untreated flour tested positive for Salmonella.
Distribution
IA, OH
Type: Voluntary: Firm initiated
Recall Initiated: 2022-02-10
Company
Denver, CO
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 70 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Ardent Mills, LLC has 2 FDA actions in our database, including 2 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 (Ardent Mills, LLC) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Ardent Mills, LLC have FDA actions?
Ardent Mills, LLC has 2 FDA actions in our database, including 2 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-0805-2022" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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