Gold Medal Bleached All Purpose Flour, Enriched, Presifted, packaged in the following sizes: 1. Net Wt 32 oz (2lb) 90
Summary
The FDA issued a Class I for Gold Medal Bleached All Purpose Flour, Enriched, Presifted, packaged in the foll by General Mills, Inc. Reason: Flour has the potential to be contaminated with Salmonella..
Details
Source
Food Recall
External ID
F-0920-2023
Action Date
2023-05-24
Status
Terminated
Category
food
Product Description
Gold Medal Bleached All Purpose Flour, Enriched, Presifted, packaged in the following sizes: 1. Net Wt 32 oz (2lb) 907g, UPC 0 16000-10710 6; and 2. Net Wt 5lb (2.26kg), UPC 0 16000-10610 9. Dist. By General Mills Sales, Inc., Minneapolis, MN 55440.
Lot/Code Info: Better if Used By 27MAR2024 and 28MAR2024
Quantity Affected: 271,454 bags
Reason for Recall
Flour has the potential to be contaminated with Salmonella.
Distribution
Nationwide
Type: Voluntary: Firm initiated
Recall Initiated: 2023-04-28
Company
Minneapolis, MN
Context & Analysis
This is a Class I recall. Class I recalls are the most serious — there is a reasonable probability that use of or exposure to the product will cause serious health consequences or death.
This was one of 74 food recalls issued in the same week, part of 204 food-related FDA actions this month.
General Mills, Inc has 2 FDA actions in our database, including 2 recalls.
Frequently Asked Questions
What is a Class I recall?
A Class I recall is the most serious type. The FDA has determined there is a reasonable probability that the product will cause serious adverse health consequences or death. Consumers should stop using the product immediately.
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 (General Mills, Inc) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does General Mills, Inc have FDA actions?
General Mills, Inc 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-0920-2023" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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