Food Recall Check
Class I · High risk Ongoing Initiated Aug 22, 2026 (2 months ago)

Everything Sprouts and Calco branded Alfalfa Sprouts recall

Recalled by Everything Sprouts, LLC · Minneapolis, MN, United States

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

Why it was recalled

Sprouts may be contaminated with STEC E. coli and/or Salmonella.

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

Everything Sprouts and Calco branded Alfalfa Sprouts, Net Wt. 5.0 oz (142 g) UPC 7 68944-00005 9. The 5 oz. containers are distributed as single units, or in a tray with 6 - 5oz containers that contains UPC 8 60014-52312 0 label on bottom of tray, or in a try with 12 - 5 oz. containers that contains UPC 8 60014-52311 3 label on bottom of tray.

Quantity: 1,830.25 pounds

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 #222, 223, 225, 226, 230

Where it was sold

Minnesota Wisconsin

FDA's distribution note: MN, 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.

Recalling firm
Everything Sprouts, LLC
Initiated by
Voluntary: Firm initiated
Recall initiated
Aug 22, 2026
In FDA report of
Sep 23, 2026
FDA recall number
H-1337-2026 · event 99737
Official record
FDA enforcement report search

Also recalled with it (3 more products)

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