Class ITerminated in FDA datasetRecall initiated May 31, 2016

50lb Sysco Classic Hotel & Restaurant Flour Bleached Enriched Malted Unit

Recalling firm: General Mills, Inc

Why it was recalled

General Mills is recalling a number of products because of a multistate outbreak of E. coli O121 that may be potentially linked to Gold Medal flour, Wondra flour, and Signature…

Historical recall record. This is not a new recall announcement. “Terminated” describes the FDA recall process; it does not certify that an individual package is safe. FDA termination date: Mar 30, 2021.

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Compare the exact product and package details with the label you have.

Product50lb Sysco Classic Hotel & Restaurant Flour Bleached Enriched Malted Unit UPC 34730-23936 Code Dates/Production Dates 17NOV5KC, 18NOV5KC 25lb Sysco All-Purpose Hotel & Restaurant Flour Bleached Enriched Malted Unit UPC 34730-23957 Code Dates/Production Dates 20NOV5KC, 21NOV5KC 25lb Sysco All-Purpose Hotel & Restaurant Flour Bleached Enriched Malted Unit UPC 34730-23958 Code Dates/Production Dates 20NOV2015KC, 21NOV2015KC
Package size50lb

FDA code information

17NOV5KC, 18NOV5KC, 20NOV5KC, 21NOV5KC

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Full FDA record and distribution details

Original product description

50lb Sysco Classic Hotel & Restaurant Flour Bleached Enriched Malted Unit UPC 34730-23936 Code Dates/Production Dates 17NOV5KC, 18NOV5KC 25lb Sysco All-Purpose Hotel & Restaurant Flour Bleached Enriched Malted Unit UPC 34730-23957 Code Dates/Production Dates 20NOV5KC, 21NOV5KC 25lb Sysco All-Purpose Hotel & Restaurant Flour Bleached Enriched Malted Unit UPC 34730-23958 Code Dates/Production Dates 20NOV2015KC, 21NOV2015KC

Original FDA recall reason

General Mills is recalling a number of products because of a multistate outbreak of E. coli O121 that may be potentially linked to Gold Medal flour, Wondra flour, and Signature Kitchens flour. To date, E. coli O121 has not been found in any General Mills flour products or in the flour manufacturing facility and the company has not been contacted directly by any consumer reporting confirmed illnesses related to these products.

Recall details

Recall number
F-2220-2016
Event ID
74285
FDA status
Terminated
Initiated
May 31, 2016
Reported
Sep 21, 2016
Classified
Sep 14, 2016
Terminated
Mar 30, 2021
Quantity
614,478 total units for all product
Location
Minneapolis, MN, United States
Initiation type
Voluntary: Firm initiated
Notification
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit

Where it was distributed

All states in US including PR, US Virgin Islands, Guam, Northern Mariana Islands except AK & SD. OUS: ARUBA, HONK KONG, CHINA , BAHAMAS, JAMAICA, BERMUDA, CURACAO, HAITI, THAILAND.

FDA source record · F-2220-2016

Data updated September 16, 2026. View official FDA data ↗

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