E-Z Spuds Inc recall

Recalled by E-Z Spuds Inc · Melrose Park, IL, United States

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

Why it was recalled

Potential contamination with Salmonella

Salmonella is the most common cause of food recalls for bacteria, often in eggs, produce, nuts and spices.

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

E-Z Spuds Inc. fresh cut onion products (10, 20, 30 lbs) diced, sliced, Julienne, whole peeled

Quantity: 5,630 cases

Food: Onions

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.

Mfg Date: JUL 14, '21 JUL 15, '21 JUL 16, '21 JUL 19, '21 JUL 20, '21 JUL 21, '21 JUL 22, '21 JUL 23, '21 JUL 26, '21 JUL 27, '21 JUL 28, '21 JUL 29, '21 JUL 30, '21 AUG 02, '21 AUG 03, '21 AUG 04, '21 AUG 05, '21 AUG 06, '21 AUG 09, '21 AUG 10, '21 AUG 11, '21 AUG 12, '21 AUG 13, '21 AUG 16, '21 AUG 17, '21 AUG 19, '21 AUG 20, '21 AUG 23, '21 AUG 24, '21 AUG 25, '21 AUG 26, '21 AUG 27, '21 AUG 30, '21 AUG 31, '21 SEP 01, '21 SEP 02, '21 SEP 03, '21 SEP 07, '21 SEP 08, '21 SEP 09, '21

Where it was sold

Illinois

FDA's distribution note: Manufacturers and Food service establishments in the Chicago, IL metro area

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: E-Z Spuds Inc
Initiated by: Voluntary: Firm initiated
Recall initiated: Oct 21, 2021
In FDA report of: Nov 17, 2021
Terminated: Jan 27, 2023
FDA recall number: F-0123-2022 · event 88916
Official record: FDA enforcement report search

Also recalled with it (9 more products)

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

Class II · Moderate risk Terminated Salmonella Oct 21, 2021