Recall record at a glance
| Official record | F-1894-2015 |
|---|---|
| Category | Food Recalls |
| Classification | Class I |
| FDA record status | Terminated |
| Recalling firm | The Santa Barbara Smokehouse, Inc. |
| Report date | Apr 15, 2015 |
| Recall initiation date | Dec 26, 2014 |
| Quantity | 29,343 lbs. |
| Location | Santa Barbara, CA, United States |
Official product description
Beechwood Smoked and Atlantic Salmon sliced sides, whole sides, and trimmings under the following brands; Coastal Harbor SKU: 8 30859 01183 0, Channel Island SKU: 8 30859 03093 0, Atlantic Smoked SKU: 8 30859 01253 0, Harbor Point SKU: 8 30859 01515 9, Local Abundance SKU: 8 30859 03075 5, Fresh & Easy 4oz. , Local Abundance SKU: 8 30859 03070 1, Fresh & Easy 4oz., Local Abundance SKU: 8 30859 03069 5, Channel Island SKU: 8 30859 03093 0 All products are vacuum packed and are either fresh or frozen. Products are cold smoked.
Why the product was recalled
The firm is recalling batches of smoked salmon due to environmental and finished product samples found positive for Listeria monocytogenes.
Distribution information
Products are sold to customers located within the U.S.; CA, NY, TX, HI, CO, MA, AZ, CT, KY, IL, NV, UT, MD, FL, MI, MO, NJ
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.