Expanded Recall: 50 lb Wondra Enriched Unmalted Flour Unit UPC 100-16000-54380 Code Dates/Production Dates 04NOV2015KC, 05NOV2015KC
⚠ Critical Alert — Stop Using Immediately
This product has been flagged with severe risks (e coli). Stop using it now and contact the brand or FDA for a refund, repair, or replacement.
FDA Recall Notice
Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-2221-2016.
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.
Corrective Action (per FDA)
Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-2221-2016.
Recall terminated by FDA.
✅ What you should do
- Stop using the product if you own it.
- Check the model number, lot code, or sell-by date against the recall notice above.
- Contact General Mills, Inc or the retailer where you bought it for a refund, replacement, or repair.
- For the most current official instructions, visit the FDA recall page.
- If you've been hurt by this product, report the incident to FDA.
Consumer Contact (per FDA)
Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-2221-2016.
General Mills, Inc
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The FDA regulates drugs, medical devices, food, cosmetics, and tobacco. Adverse event reports and recall notices are the main public safety signal.
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If you had a reaction, found contamination, or experienced a labeling problem with this product, report it to the FDA. The agency uses consumer reports to track emerging safety signals and trigger recalls.
General Mills, Inc Recall FAQ
General Mills, Inc is the subject of a food safety report: Expanded Recall: 50 lb Wondra Enriched Unmalted Flour Unit UPC 100-16000-54380 Code Dates/Production Dates 04NOV2015KC, 05NOV2015KC. The notice was published on May 31, 2016 by the U.S. Food and Drug Administration (FDA). Approximately 614,478 units are potentially affected.