Class IITerminated in FDA datasetJan 28, 2013

Wheatgrass is packaged in a pint or cup

Recalling firm: Giant Greens, Inc.

Why it was recalled

Wheatgrass is recalled due to a potential contamination with Listeria monocytogenes.

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The exact product

Wheatgrass is packaged in a pint or cup, 16 oz. bag, or 5 lb. Flat cardboard box and sold under the Sprouters Northwest brand. The Wheatgrass in a pint or cup has UPC 0 79566 12380 5; The wheatgrass in 16 oz. bag or 5 lb. Flat cardboard box does not have any UPC. The wheatgrass, Sprouters Northwest, pint or cup., is labeled in parts: "***Wheatgrass***CERTIFIED ORGANIC***Pint***Sprouters NORTHWEST, INC.***KENT, WA 98032***". The wheatgrass in 16 oz. bag is labeled in parts: "***ORGANIC WHEATGRASS***SKU# 16OZCW***Keep Refrigerated***Not For Retail Sales as Packaged***". The wheatgrass in 5 lb. Flat cardboard box is labeled in parts: "***Wheatgrass***1 Ea. 21"X21" Wheatgrass/case***Item 40019***".

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

The Best by Dates are including all and up to 2/17/2013

TypeCode / valueContext
UPC079566123805nder the Sprouters Northwest brand. The Wheatgrass in a pint or cup has UPC 0 79566 12380 5; The wheatgrass in 16 oz. bag or 5 lb. Flat cardboard box does not have any UPC. The wheatgrass, Sprouters Northw

Recall details

Recall number
F-1018-2013
Event ID
64203
FDA status
Terminated
Initiated
Jan 28, 2013
Reported
Mar 6, 2013
Classified
Feb 26, 2013
Terminated
Mar 20, 2013
Quantity
3024/1 pint Packages; 888 cups; 63/16 oz. Bags; and 494/5 lbs. Flat boxes;
Location
Kent, WA, United States
Initiation type
Voluntary: Firm initiated
Notification
Press Release

Where it was distributed

Products distributed in Alaska, Idaho, Oregon, Washington, and British Columbia, Canada.

FDA source record · F-1018-2013

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.