Food Recall Check
Class II · Moderate risk Terminated Initiated Feb 18, 2016 (11 years ago)

Watts Brothers FARMS SUPERSWEET CUT CORN*** recall

Recalled by ConAgra Foods Inc · Omaha, NE, United States

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

ConAgra is recalling one lot of Watts Bros Super Sweet Cut Corn bulk packed, due to the 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

Label reads in part "***Watts Brothers FARMS SUPERSWEET CUT CORN***NET WT 20 LB*** Distributed by ConAgra Foods Kennewick, WA 99336 PRODUCT OF U.S.A.***" Product is blanched then frozen and placed in a plastic lined cardboard box. UPC 1 06 81241 05167 8

Quantity: 3298 cs - 20lbs/cs

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.

Lot code on package P: 2015. 12. 05. Manufacturing date December 5, 2015. Expiration date December 5, 2017 (E: 2017. 12. 05).

Where it was sold

California Michigan Oregon Tennessee

FDA's distribution note: CA, MI, OR and TN. No distribution to schools or military. No distribution outside the U.S.

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
ConAgra Foods Inc
Initiated by
Voluntary: Firm initiated
Recall initiated
Feb 18, 2016
In FDA report of
Mar 30, 2016
Terminated
Oct 17, 2016
FDA recall number
F-0794-2016 · event 73335
Official record
FDA enforcement report search

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