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High RiskFDAfda-F-1252-2014OTHER

Self-Rising White Cornmeal Mix sold under the Aunt Jemima brand and packaged in a paper bag with a net weight respectively of 32 oz. (2 l...

Category
Units Affected
15,334
Recall Date
October 29, 2013
Issuing Agency
Hazard
Other

FDA Recall Notice

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-1252-2014.

Some Aunt Jemima and Quaker brand Self-Rising Corn Meal Mix, Buttermilk Self-Rising Corn Meal Mix, and Quick Grits have levels of aflatoxin above the legal limit.

Corrective Action (per FDA)

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-1252-2014.

Recall terminated by FDA.

✅ What you should do

  1. Stop using the product if you own it.
  2. Check the model number, lot code, or sell-by date against the recall notice above.
  3. Contact Quaker Foods And Snacks North America or the retailer where you bought it for a refund, replacement, or repair.
  4. For the most current official instructions, visit the FDA recall page.
  5. 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-1252-2014.

Quaker Foods and Snacks North America

FDA

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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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📣 Report a food, supplement, or cosmetic problem to the FDA

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.

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Quaker Foods And Snacks North America Recall FAQ

Quaker Foods And Snacks North America is the subject of a food safety report: Self-Rising White Cornmeal Mix sold under the Aunt Jemima brand and packaged in a paper bag with a net weight respectively of 32 oz. (2 l.... The notice was published on October 29, 2013 by the U.S. Food and Drug Administration (FDA). Approximately 15,334 units are potentially affected.