Wild Mushroom in Phyllo recall

Recalled by Kabobs Inc · Lake City, GA, United States

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

Why it was recalled

Product was manufactured with flour recalled due to E. coli O121 contamination.

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

WILD MUSHROOM IN PHYLLO, 100 CT and 200 CT, Prepared by: Kabobs, 54234 North Lake Dr. Lake City, GA 30260.

Quantity: 10 cases (200 units per case)

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.

Item number: K751, Lot/Julian Code: PM16A13 / 16013 and Item number: K7515, Lot/Julian Code: PM15M16 / 15350..

Where it was sold

Arkansas California Colorado Connecticut Florida Georgia Illinois Indiana Kentucky Louisiana Massachusetts Maryland Michigan Minnesota Missouri North Carolina New Jersey Nevada New York Ohio Oklahoma Oregon Pennsylvania Tennessee Texas Washington Wisconsin

FDA's distribution note: AR, CA, CO, CT, FL, GA, IL,IN, IO, KY, LA, MA, MD, MI, MN, MO, NC, NJ, NY, NV, OK, OH, OR, PA, TN, TX WA, and WI.

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: Kabobs Inc
Initiated by: Voluntary: Firm initiated
Recall initiated: Jul 6, 2016
In FDA report of: Oct 26, 2016
Terminated: Nov 6, 2017
FDA recall number: F-0135-2017 · event 74686
Official record: FDA enforcement report search

Also recalled with it (26 more products)

FDA files each product of one recall action separately; these share the same FDA event.

Class II · Moderate risk Terminated E. coli Jul 6, 2016