Kellogg's Honey Smacks
Reason Kellogg North America initiated a voluntary recall of Kellogg s Honey Smacks, 15.3 oz. and 23 oz., due to potential contamination with Salmonella.
Kelloggs ¿ Eggo ¿ Nutri-Grain¿ Whole Wheat Waffles recall
Recalled by Kellogg Company · Battle Creek, MI, United States
Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.
Why it was recalled
Potential to be contaminated with Listeria monocytogenes.
Pathogen: Listeria
Listeria monocytogenes can grow even in the fridge and is especially dangerous in pregnancy.
The most serious food recalls: a contaminated product can cause outbreaks, hospitalisations and deaths, especially for pregnant people, young children, older adults and anyone with a weakened immune system. All bacteria & viruses recalls.
What was recalled
Kelloggs ¿ Eggo ¿ Nutri-Grain¿ Whole Wheat Waffles 12.3 oz (10 ct) retail carton 8, 12.3 oz retail cartons per case
Quantity: 10,950 Cases
Lot codes, dates and UPCs
A recall covers only these codes. Compare them with the lot number, best-by date or UPC printed on your package.
UPC: 38000 40370 Better If Used Before Date: NOV21 17 ER and NOV22 17 ER The date code can be found on the side of the package.
Where it was sold
Colorado Connecticut Delaware Georgia Iowa Illinois Indiana Kansas Massachusetts Maryland Maine Michigan Minnesota Missouri North Dakota Nebraska New Hampshire New Jersey New York Ohio Pennsylvania Virginia Vermont Wisconsin Wyoming
FDA's distribution note: CO, CT, DE, GA, IA, IL, IN, KS, MA, MD, ME, MI, MN, MO, ND, NE, NH, NJ, NY, OH, PA, VA, VT, WI, WY
Check the codes, then return or discard. Class II means eating it may cause temporary or reversible health problems. If your package matches the recalled codes, do not eat it - return it to the store or throw it away. FDA lists this recall as terminated: the company has finished removing the product, so it should no longer be on shelves - but it can still be in a freezer or pantry.
- Recalling firm
- Kellogg Company
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Sep 19, 2016
- In FDA report of
- Oct 19, 2016
- Terminated
- Mar 24, 2017
- FDA recall number
- F-0050-2017 · event 75223
- Official record
- FDA enforcement report search
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