BBU Fine Whole Wheat Flour Bulk-AA-50251, Bulk Tanker; SG Whole Wheat Fine Flour 2,000 lb. Tote-AA Storage instruc
Summary
The FDA issued a Class II for BBU Fine Whole Wheat Flour Bulk-AA-50251, Bulk Tanker; SG Whole Wheat Fine Fl by Ardent Mills, LLC. Reason: Potential to contain small pieces of stainless steel from a piece of milling equipment which was discovered during an investigative inspection of our .
Details
Source
Food Recall
External ID
F-1090-2022
Action Date
2022-06-08
Status
Terminated
Category
food
Product Description
BBU Fine Whole Wheat Flour Bulk-AA-50251, Bulk Tanker; SG Whole Wheat Fine Flour 2,000 lb. Tote-AA Storage instructions - Any product made from raw agricultural commodities, such as wheat, rye and other grains, may be subject to infestation if not properly inspected when received, handled, and stored. To reduce the risk of infestation, customer should ensure it has proper goods receiving inspection procedures, and should store the product in a clean, dry area that is well ventilated
Lot/Code Info: BBU Fine WW Flour Bulk - 0083840839; SG WW Fine Flour Tote-AA - 918345; 918346
Quantity Affected: 126,900 lbs. total
Reason for Recall
Potential to contain small pieces of stainless steel from a piece of milling equipment which was discovered during an investigative inspection of our system.
Distribution
CA, IA
Type: Voluntary: Firm initiated
Recall Initiated: 2022-05-18
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 76 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-1090-2022" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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