Recall record at a glance
| Official record | F-1317-2022 |
|---|---|
| Category | Food Recalls |
| Classification | Class I |
| FDA record status | Terminated |
| Recalling firm | Euphoria Trading Company, LLC. |
| Report date | Jun 22, 2022 |
| Recall initiation date | May 24, 2022 |
| Quantity | 771 Dark Chocolate Peanut Butter Meltaways; |
| Location | Eugene, OR, United States |
Official product description
Dark Chocolate Peanut Butter Meltaways are rectangular bars with the filling consisting of crunchy peanut butter and milk chocolate and are then dipped in dark chocolate. Net wt. is approximately 1.25oz. UPC 5046901342. Each box consists of 70 pieces and they are not meant for retail sale and do not have the firm name and address listed. The product is put into display cases and will be packed at the time of sale.
Why the product was recalled
Potential contamination with Salmonella. Product contains Jif peanut butter.
Distribution information
Distributed in Oregon
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.