FDA Food Recalls

Recalls / Class I

Class IF-2214-2016

Class I— FDA's most serious classification, issued when there is a reasonable probability that consumption of or exposure to the product will cause serious adverse health consequences or death.

Product

2 lb Gold Medal Self Rising Flour Case UPC 000-16000-10730 Package UPC 000-16000-11710 Recalled Better If Used By Dates 23AUG2016KC Expanded: 09AUG2016KC, 10AUG2016KC, 16AUG2016KC, 17AUG2016KC, 06SEP2016KC, 07SEP2016KC Expanded Recall: 5 lb Gold Medal Self Rising Flour Package UPC 000-16000-11610 Recalled Better if Used by Dates 10AUG2016KC, 11AUG2016KC Expanded Recall #2 7-25-16 Recalled Better if Used by Dates 27OCT2016KC

Type
Food
Affected lot / code info
23AUG2016KC Expanded Recall: 09AUG2016KC, 10AUG2016KC, 16AUG2016KC, 17AUG2016KC, 06SEP2016KC, 07SEP2016KC, 11AUG2016KC. Expanded Recall #2 7-25-16 Recalled Better if Used by Dates 27OCT2016KC
Quantity
614,478 total units for all product

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 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.

Recalling firm

Firm
General Mills, Inc
Notification channel
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Type
Voluntary: Firm initiated
Address
1 General Mills Blvd, N/A, Minneapolis, Minnesota 55426-1347

Distribution

Distribution pattern
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.

Timeline

Recall initiated
2016-05-31
FDA classified
2016-09-14
Posted by FDA
2016-09-21
Terminated
2021-03-30
Status
Terminated

Source: openFDA Food Enforcement endpoint. Recall record F-2214-2016. The FDA issues recall classifications as health-hazard assessments, not legal findings.