Food Recall Check
Class I · High risk Terminated Initiated Nov 2, 2021 (5 years ago)

Alsum Farms & Produce Whole White Onions recall

Recalled by Alsum Farms & Produce, Inc. · Friesland, WI, United States

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

Why it was recalled

Onions are being recalled by Keeler Family Farms due to potential Salmonella contamination.

Pathogen: 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

Alsum Farms & Produce Whole White Onions, 2 lbs. (907g) UPC 39186-60051. Produce of Mexico. Packed by Alsum Farms & Product, Inc., Friesland, WI 53935.

Quantity: 252 bags

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.

Lot 169008

Where it was sold

Illinois Michigan Pennsylvania Wisconsin

FDA's distribution note: IL, MI, PA, WI

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
Alsum Farms & Produce, Inc.
Initiated by
Voluntary: Firm initiated
Recall initiated
Nov 2, 2021
In FDA report of
Dec 8, 2021
Terminated
Jan 13, 2022
FDA recall number
F-0225-2022 · event 89043
Official record
FDA enforcement report search

Also recalled with it (2 more products)

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

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