Recall record at a glance
| Official record | F-0163-2017 |
|---|---|
| Category | Food Recalls |
| Classification | Class I |
| FDA record status | Terminated |
| Recalling firm | Fred Meyers Inc. |
| Report date | Oct 26, 2016 |
| Recall initiation date | Sep 30, 2016 |
| Quantity | unknown- firm did not provide |
| Location | Portland, OR, United States |
Official product description
Product is refrigerated Boars Head To Go (BTG) Superfood Wrap, sold at deli department. The wraps are made in store and the weight varies and they are sold as one each (wrap). The UPC is 41573 11053.
Why the product was recalled
Deli Boars Head To Go (BTG) Superfood Wrap was recalled due to undeclared milk, soybeans (edamame), wheat and cashews.
Distribution information
distributed at Fred Meyer stores in in Alaska, Idaho, Oregon and Washington.
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
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.