Food Recall Check
Class I · High risk Terminated Initiated Aug 23, 2012 (14 years ago)

Champ's Sliced White Mushrooms recall

Recalled by Spokane Produce, Inc. · Spokane, WA, United States

Class I — High risk. Reasonable probability of serious harm or death.

Why it was recalled

Product recalled due to potential contamination 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

Champ's Sliced White Mushrooms, 227 g/8 oz, in a styrofoam container with shrink wrap, UPC 0 33383 67600 5. Labeled in part: "CHAMP'S MUSHROOMS Sliced White Mushrooms, Product of Canada, 227g/8 oz, 0 33383 67600 5 KEEP REFRIGERATED

Quantity: 140 cases (1,260 - 8 ounce containers)

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.

Packed on Date is PO 11AUG2012. The Best Before is 22AUG2012. Date code is the packed on date and product has a 10 day shelf life with the pack on date being day one.

Where it was sold

Idaho Montana Oregon Washington Wyoming

FDA's distribution note: Washington, Idaho, Montana, Oregon, Wyoming and 9 military bases.

Do not eat it. Class I means FDA judged there is a reasonable probability of serious illness or death. If the brand, size and lot or date code on your package match, throw the product away or return it to the store for a refund, and clean any surface or container it touched. If anyone has eaten it and feels unwell, contact a doctor and mention the recall. 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
Spokane Produce, Inc.
Initiated by
Voluntary: Firm initiated
Recall initiated
Aug 23, 2012
In FDA report of
Oct 10, 2012
Terminated
Oct 25, 2012
FDA recall number
F-0013-2013 · event 62996
Official record
FDA enforcement report search

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