Recall record at a glance
| Official record | F-2331-2012 |
|---|---|
| Category | Food Recalls |
| Classification | Class I |
| FDA record status | Terminated |
| Recalling firm | Somersault Snack Co., LLC |
| Report date | Sep 26, 2012 |
| Recall initiation date | Aug 31, 2012 |
| Quantity | 418 cases of 12.6oz packages |
| Location | Sausalito, CA, United States |
Official product description
Somersaults Crunchy Nuggets baked with sunflower seed and toasted grains. Pacific Sea Salt Flavor, Net Wt. 6 oz. UPC 8-98403 00201-7;
Why the product was recalled
Consumer complaints and subsequent investigation found that packages of Pacific Sea Salt snack crackers had some Santa Fe Salsa snack crackers mixed in. Santa Fe Salsa crackers contain milk protein which is not declared on the ingredient labeling.
Distribution information
CA, NH, NV, RI, MD, PA, TN, FL, CT. WA, TX, NJ, MN, IN, GA.
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.