Fire roasted Poblano & Jalapeno popper bites packaged in a white box with black lettering
Reason Firm used Flour from General Mills that has been contaminated with E. Coli O121.
Breaded stuffed Jalapenos poppers labeled in part recall
Recalled by McCain Foods USA · Lisle, IL, United States
Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.
Why it was recalled
Firm used Flour from General Mills that has been contaminated with E. Coli O121.
Pathogen: E. coli
Shiga toxin-producing E. coli (such as O157:H7) can cause severe illness and kidney failure.
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
Breaded stuffed Jalapenos poppers labeled in part: Anchor breaded Fiesta Bold Poppers, breaded stuffed jalapenos, keep frozen. The product is packaged in a green 4 lb. box with white, green and orange lettering.
Quantity: 555 cases ( 2, 4 lb. boxes per case)
Food: Bread & bakery
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.
30010718
Where it was sold
Nationwide.
FDA's distribution note: Nationwide. There are no foreign consignees.
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
- McCain Foods USA
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Jul 12, 2016
- In FDA report of
- Sep 14, 2016
- Terminated
- Apr 22, 2019
- FDA recall number
- F-2097-2016 · event 74718
- Official record
- FDA enforcement report search
Also recalled with it (1 more product)
FDA files each product of one recall action separately; these share the same FDA event.
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