Krusteaz Blueberry Pancake Mix, 28 oz. carton, UPC code 041449001289 Krusteaz Blueberry Pancake Mix, 3.5 lb. bag, UPC code 041449...
⚠ 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-2141-2016.
Krusteaz Blueberry Pancake Mix is recalled due to a potential to be contaminated with E. coli O121.
Corrective Action (per FDA)
Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-2141-2016.
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 Continental Mills (corporate Office) 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-2141-2016.
Continental Mills (Corporate Office)
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.
Continental Mills (corporate Office) Recall FAQ
Continental Mills (corporate Office) is the subject of a bakery & grains safety report: Krusteaz Blueberry Pancake Mix, 28 oz. carton, UPC code 041449001289 Krusteaz Blueberry Pancake Mix, 3.5 lb. bag, UPC code 041449.... The notice was published on July 7, 2016 by the U.S. Food and Drug Administration (FDA). Approximately 48,260 units are potentially affected.