Recall record at a glance
| Official record | F-1882-1015 |
|---|---|
| Category | Food Recalls |
| Classification | Class I |
| FDA record status | Terminated |
| Recalling firm | Texamerican Food Blending, Inc. |
| Report date | Apr 15, 2015 |
| Recall initiation date | Dec 24, 2014 |
| Quantity | 20,000 pounds |
| Location | Hot Springs, AR, United States |
Official product description
Texamerican Roast Dip Seasoning 50 lbs. Item Number TF25004
Why the product was recalled
Texamerican Food Blending received notification from its supplier that two lots of ingredients were contaminated with Peanut allergen. The products affected do not have peanuts listed in the ingredient statement. All product items listed have a cleanout after mixing. The firm current corrective action in regard to receiving this ingredient is to discontinue ordering ingredient from Schiff Foo
Distribution information
AR, OK, TX, TN
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: Letter.
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.