Food Recall Check
Class I · High risk Terminated Initiated Nov 1, 2012 (14 years ago)

Wegmans Organic Spinach & Spring Mix --- Product is packaged in clam shell in two sizes recall

Recalled by Wegmans Food Markets · Rochester, NY, United States

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

Why it was recalled

Wegmans has recalled 5 oz. and 11 oz. packages of Organic Spinach and Spring Mix Blend because the product may be contaminated with E. coli O157:H7.

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

Wegmans Organic Spinach & Spring Mix --- Product is packaged in clam shell in two sizes: 5oz and 11oz.

Quantity: 31,000 lbs

Food: Leafy greens & salads Seafood & fish

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.

All lot codes sold between October 14, 2012 and November 1, 2012.

Where it was sold

Massachusetts Maryland New Jersey New York Pennsylvania Virginia

FDA's distribution note: New York, Pennsylvania, New Jersey, Virginia, Maryland, and Massachusetts

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
Wegmans Food Markets
Initiated by
Voluntary: Firm initiated
Recall initiated
Nov 1, 2012
In FDA report of
Jan 30, 2013
Terminated
May 8, 2017
FDA recall number
F-0915-2013 · event 63893
Official record
FDA enforcement report search

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