Recall record at a glance
| Official record | F-1018-2013 |
|---|---|
| Category | Food Recalls |
| Classification | Class II |
| FDA record status | Terminated |
| Recalling firm | Giant Greens, Inc. |
| Report date | Mar 6, 2013 |
| Recall initiation date | Jan 28, 2013 |
| Quantity | 3024/1 pint Packages; 888 cups; 63/16 oz. Bags; and 494/5 lbs. Flat boxes; |
| Location | Kent, WA, United States |
Official product description
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***".
Why the product was recalled
Wheatgrass is recalled due to a potential contamination with Listeria monocytogenes.
Distribution information
Products distributed in Alaska, Idaho, Oregon, Washington, and British Columbia, Canada.
How to read the classification
FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.
Additional record details
Recall type: Voluntary: Firm initiated. Initial notification: Press Release.
What to do next
If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.
About this record
Recall Lookup USA preserves the most complete source information successfully retrieved. We do not create missing facts or infer affected lots or VINs. The official record may still change, so use the identifier above when verifying current instructions.
FDA source limitation: openFDA enforcement reports are a reference dataset, not a live public-alert or recall-lifecycle service. FDA notes that enforcement-report status may not be updated after classification. Confirm current actions with the FDA, recalling firm or appropriate healthcare professional when relevant.