Betty Crocker Delights Super Moist Carrot Cake Mix, NET WT 15.25 OZ (432 g), Package UPC 1 00 16000 40987 0, Carton UPC: 000-16000-40987 0.
⚠ 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-2287-2016.
Three flavors of Betty Crocker cake mix are being recalled by General Mills because of possible contamination with E. coli O121 associated with Gold Medal Flour recall.
Corrective Action (per FDA)
Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-2287-2016.
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-2287-2016.
General Mills, Inc
About the U.S. Food and Drug Administration
The FDA regulates drugs, medical devices, food, cosmetics, and tobacco. Adverse event reports and recall notices are the main public safety signal.
Visit FDA.gov →📣 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.
General Mills, Inc Recall FAQ
General Mills, Inc is the subject of a bakery & grains safety report: Betty Crocker Delights Super Moist Carrot Cake Mix, NET WT 15.25 OZ (432 g), Package UPC 1 00 16000 40987 0, Carton UPC: 000-16000-40987 0.. The notice was published on July 11, 2016 by the U.S. Food and Drug Administration (FDA). Approximately 156,370 units are potentially affected.