Recall record at a glance
| Official record | F-1010-2013 |
|---|---|
| Category | Food Recalls |
| Classification | Class I |
| FDA record status | Terminated |
| Recalling firm | Giant Greens, Inc. |
| Report date | Mar 6, 2013 |
| Recall initiation date | Jan 28, 2013 |
| Quantity | 14154/4 oz. Packages; 5130/5 oz. Packages; 24287/1 lb. Bags; and 552/2 lb. Trays |
| Location | Kent, WA, United States |
Official product description
Clover sprouts, product is packaged in a 4 oz or 5 oz. clamshell containers, and 1 lb. bag or 2 lb. tray. Product is sold under brand Sprouters Northwest. Clover Sprouts, 4oz container, has a UPC 8 15098 00201 6; Clover Sprouts, 5oz container, has a UPC 0 33383 70235 3; Clover Sprouts, 1 lb bag, has a UPC 0 79566 12351 5; Clover Sprouts, 2 lb tray, has a UPC 0 79566 12351 5; The Clover Sprouts, 4 oz., Sprouters Northwest brand is labeled in parts: "***CLOVER SPROUTS***Sprouters NORTHWEST***NET WT 4.0 oz***KEEP REFRIGERATED***DISTRIBUTED BY: SPROUTERS NORTHWEST, KENT, WA 98032***www.SproutersNorthwest.com***". The Clover Sprouts, 5 oz., Sprouters Northwest brand is labeled in parts: "***CLOVER ***Sprouters NORTHWEST, INC. KENT, WA 98032***NET WT 5.0 oz***KEEP REFRIGERATED***". The Clover Sprouts, 1 LB., Sprouters Northwest brand is labeled in parts: "***CLOVER SPROUTS***NET WT. 1 LB***KEEP REFRIGERATED***Sprouters NORTHWEST, KENT, WA 98032***". The Clover Sprouts, 2 LB., Sprouters Northwest brand is labeled in parts: "***Clover Sprouts***2 lb.*** Sprouters NORTHWEST, KENT, WA 98032***".
Why the product was recalled
Clover sprouts are 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 I indicates a situation in which there is a reasonable probability that use of or exposure to the product will cause serious adverse health consequences or death. The classification shown here comes directly from the FDA enforcement 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
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