Recall record at a glance
| Official record | F-0155-2018 |
|---|---|
| Category | Food Recalls |
| Classification | Class I |
| FDA record status | Terminated |
| Recalling firm | Earthbound Farm, LLC |
| Report date | Nov 8, 2017 |
| Recall initiation date | Oct 21, 2017 |
| Quantity | 1,755 cases |
| Location | San Juan Bautista, CA, United States |
Official product description
Earthbound Farm Organic Chopped Asian Style Salad Kit; 11 oz. bag; (Salad and toppings 8.5 oz {241g} dressing 2.41 fl. oz. [71 mL]). Ingredients: Cabbage, Romaine lettuce, Kale, Carrots, Cilantro, Crunchy toppings and Tahini Dressing. UPC 32601 95134 Earthbound Farms, San Juan Bautista, CA 95045
Why the product was recalled
Recall of Asian Style Chopped Salad Kit because in some instances the dressing and toppings packets inside the bag are not those foe the salad. Some of the Asian Style Salad Kits could have the dressing packet for the Southwest Chopped Salad Kit which contains egg and milk that are not declared as ingredients on the bag of the Asian Style Salad Kit.
Distribution information
Alaska, Arizona, California, Colorado, Florida, Georgia, Hawaii, Iowa, Illinois, Indiana, Kansas, Kentucky, Massachusetts, Maryland, Michigan, Minnesota, Missouri, North Carolina, North Dakota, New York, Oklahoma, Oregon, Pennsylvania, South Carolina, Texas, Utah, Virginia, Washington, Wisconsin.
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: Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit.
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.