Food, drugs, devices › General Mills, Inc
Food recall: Gold Medal Unbleached All Purpose Flour. Net Wt 5 lb. (2.26kg). UPC 16000-19610. Distributed By General Mills Sales, Inc
General Mills, Inc (Minneapolis, MN) initiated this food recall on 23 Jan 2019; FDA lists 1 product record under event 81969, classified Class II.
FDA defines Class II as a situation in which use of or exposure to a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote. 56% of the 516 food enforcement events initiated in 2019 carry the same class.
Status: Terminated, terminated 21 Jan 2020. Initiation: voluntary: firm initiated. General Mills, Inc has 21 enforcement events on this register, with a median of 1 product record per event.
Recall classification reflects the relative degree of health hazard. Text in quotation marks is FDA's. openFDA export dated 28 Sep 2026.
Recalling firm
General Mills, Inc, Minneapolis, MN.
Reason for recall
"Gold Medal Unbleached All Purpose 5 lb. flour is being recalled due to potential Salmonella contamination."
Distribution
"AL, CO, CT, FL, GA, IL, IN, KY, MI, MN, MO, MS, NC, NJ, NY, OH, PA, TNN, VA, VT, WI."
Product records
| Recall number | Product | Quantity | Class | Status | Report date |
|---|---|---|---|---|---|
| F-0844-2019 | Gold Medal Unbleached All Purpose Flour. Net Wt 5 lb. (2.26kg). UPC 16000-19610. Distributed By General Mills Sales, Inc., Minneapolis, MN 55440 Cook Before Sneaking a Taste. Flour is Raw. Please Cook Fully Before Enjoying. | 89,571 units | Class II | Terminated | 13 Feb 2019 |
Context
Other enforcement events for General Mills, Inc
All 21 events for General Mills, Inc
Questions and answers
Why was this food recalled?
FDA's record gives the reason for recall as: "Gold Medal Unbleached All Purpose 5 lb. flour is being recalled due to potential Salmonella contamination."
What does Class II mean?
FDA classifies recalls by relative degree of health hazard. Class II is a situation in which use of or exposure to a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote.
Where was the product distributed?
FDA's distribution pattern field reads: "AL, CO, CT, FL, GA, IL, IN, KY, MI, MN, MO, MS, NC, NJ, NY, OH, PA, TNN, VA, VT, WI."
Is the recall still ongoing?
FDA lists the status as Terminated; the termination date is 21 Jan 2020. "Terminated" means FDA has determined that all reasonable efforts to remove or correct the product have been made.
Where does this data come from?
openFDA enforcement reports (food, drug and device), CC0, export dated 28 Sep 2026. Text in quotation marks is FDA's. The FDA enforcement report linked above is authoritative.
Provenance
Source: openFDA food enforcement reports (CC0), export dated 28 Sep 2026; records grouped by FDA event number. The class shown for the event is the most severe class among its records. Errors in processing are corrected at the next build; see corrections.