RecallRadar
FDA · FoodClass I

Jack & The Green Sprouts, Inc. food recall: Jack & the Green Sprouts Alfalfa Sprouts

ListeriaMicrobial contamination

Key facts

Agency
U.S. Food and Drug Administration (FDA)
Program
Food
Classification
Class I
Status
Ongoing
Event ID
96257
Recall initiated
Feb 6, 2025
Classified by FDA
Feb 19, 2025
Posted in Enforcement Report
Feb 26, 2025
Recalling firm
Jack & The Green Sprouts, Inc.
Firm location
River Falls, WI, United States
Initiated by
Voluntary: Firm initiated
Firm notified customers by
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Products in this event
1

What to do

Compare the product name, size, UPC, lot codes and dates below with the product you have. If it matches, do not eat it. Follow the firm's instructions to return it or throw it away.

View the official FDA record ↗

Reason for recall

Sprouts have the potential to be contaminated with Listeria monocytogenes

What the classification means

  • Class I: FDA's most serious category: there is a reasonable probability that using or being exposed to the product will cause serious health problems or death.

About this recall

The firm started this recall on Feb 6, 2025. FDA classified it 13 days later, on Feb 19, 2025. Distribution reported by FDA: IA, MN, WI Jack & The Green Sprouts, Inc. has 2 recalls in our records.

Recalled products (1)

  • F-0569-2025 Class I Ongoing

    Jack & the Green Sprouts Alfalfa Sprouts. Net Weight 5 oz. (152g). UPC 7 63247-19891 5. Keep Refrigerated. Product of USA. River Falls, WI 54022.

    Codes / lots: Lot # 687

    Quantity: 2,688 units

Source and freshness

Source
U.S. Food and Drug Administration (FDA) Enforcement Report, via the openFDA food enforcement dataset
Official notice
FDA Enforcement Report, event 96257
Raw record
openFDA API (JSON)
Dataset last updated by FDA
Nov 3, 2026
Imported by RecallRadar
Nov 4, 2026

Enforcement Report entries describe recalls FDA has classified. They are not always the same as a company press release. If something here differs from FDA's record, FDA's record is correct — please tell us.