Recall record at a glance
| Official record | F-0570-2013 |
|---|---|
| Category | Food Recalls |
| Classification | Class I |
| FDA record status | Terminated |
| Recalling firm | Xan Confections |
| Report date | Nov 7, 2012 |
| Recall initiation date | Oct 1, 2012 |
| Quantity | 40 cases |
| Location | Irvine, CA, United States |
Official product description
Chocolate, confections. Bulk Dark Mini BigMouth, item number 094. Each case contains 15 pieces.
Why the product was recalled
The firm voluntarily recalled 13 of its gourmet peanut butter chocolate products because they have the potential to be contaminated with Salmonella, upon learining that Sunland, Inc., the peanut butter supplier used in the production of Xan Confections, has recalled its entire peanut butter product from May 1, 2012 throught September 24, 2012.
Distribution information
The recall affected Xan Confections products distributed through 98 stores in California, Arizona, Nevada, Oregon, Washington, Texas, Alabama, Louisiana and Nova Scotia (Canada), as well as through online distribution.
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: FAX.
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.