Recall record at a glance
| Official record | F-1399-2015 |
|---|---|
| Category | Food Recalls |
| Classification | Class I |
| FDA record status | Terminated |
| Recalling firm | First Spice Mixing Co., Inc. |
| Report date | Mar 18, 2015 |
| Recall initiation date | Dec 24, 2014 |
| Quantity | Lot 2481405: 25 lbs., Lot 3071409: 25 lbs. |
| Location | Long Island City, NY, United States |
Official product description
SALSA PICA ASADA (SEA-268), Net Weight XXXX Lbs. -- FIRST SPICE MIXING COMPANY LONG ISLAND CITY, N.Y. --- INGREDIENTS: SALT, SPICES, SUGAR, PAPRIKA, CITRIC ACID, GARLIC POWDER, DEHYDRATED ONION. --- The % of cumin used in the finished seasoning mix is 4.50%. --- The affected lots were shipped on 9/5/14 and 11/7/14.
Why the product was recalled
Firm was notified by immediate supplier that certain lots of ground cumin may have been contaminated with peanut protein which is not declared on the label.
Distribution information
NY, PA, OH, MA, RI, NJ, WI
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: E-Mail.
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.