Class ICompleted in FDA datasetOct 1, 2024

Jack & the Green Sprouts Alfalfa, Net Weight 5 oz (142g).

Recalling firm: Jack & The Green Sprouts, Inc.

Why it was recalled

Sprouts may be contaminated with Listeria monocytogenes.

Check the codes ↓

The exact product

Jack & the Green Sprouts Alfalfa, Net Weight 5 oz (142g). UPC 7 63247-19891 5 Keep Refrigerated. Product of USA. Jackandthegreensprouts.com, River Falls, WI 54022. EXPANDED 10/4/2024: Product was packaged in 5 oz containers that were packed in 6 count or 12 count shipping containers, or in a 5lb. bulk tray. Bulk trays are a black plastic growing tray inside a poly bag fastened with a twist tie. One tray per shpper box.

Check the codes

Compare these FDA-provided codes, lot numbers or dates with the product you have.

Match the product, size and code together. A similar name alone does not identify your batch.

Original FDA code information

Lot # 048 and 777. Expiration Dates 9/18/24 and 9/25/24 Expanded 10/4/2024: Lot # 300 Expiration 10/9/24 and Lot # 246 Expiration 10/11/24.

TypeCode / valueContext
UPC763247198915Jack & the Green Sprouts Alfalfa, Net Weight 5 oz (142g). UPC 7 63247-19891 5 Keep Refrigerated. Product of USA. Jackandthegreensprouts.com, River Falls, WI 54022. EXPANDED 10/4/2024: Produ
expiration10/11/24/24 Expanded 10/4/2024: Lot # 300 Expiration 10/9/24 and Lot # 246 Expiration 10/11/24.
expiration10/9/24 Expiration Dates 9/18/24 and 9/25/24 Expanded 10/4/2024: Lot # 300 Expiration 10/9/24 and Lot # 246 Expiration 10/11/24.
lot246/18/24 and 9/25/24 Expanded 10/4/2024: Lot # 300 Expiration 10/9/24 and Lot # 246 Expiration 10/11/24.
lot300 048 and 777. Expiration Dates 9/18/24 and 9/25/24 Expanded 10/4/2024: Lot # 300 Expiration 10/9/24 and Lot # 246 Expiration 10/11/24.

Recall details

Recall number
F-0073-2025
Event ID
95470
FDA status
Completed
Initiated
Oct 1, 2024
Reported
Nov 6, 2024
Classified
Oct 28, 2024
Quantity
1,501 units EXPANDED 10/04/2024: 9,580 units and 48 trays (total)
Location
River Falls, WI, United States
Initiation type
Voluntary: Firm initiated
Notification
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit

Where it was distributed

IA, MN, WI

FDA source record · F-0073-2025

Data updated September 16, 2026. View official FDA data ↗

A missing code match is not a guarantee of safety. Follow official FDA and manufacturer guidance.