Recall record at a glance
| Official record | F-0907-2017 |
|---|---|
| Category | Food Recalls |
| Classification | Class I |
| FDA record status | Terminated |
| Recalling firm | Western United Fish Company, Inc. |
| Report date | Jan 4, 2017 |
| Recall initiation date | Nov 5, 2016 |
| Quantity | 1044 kits (4.35 lbs. per kit) |
| Location | Redmond, WA, United States |
Official product description
Limu Poke is fresh refrigerated product, distributed in bulk kit, net wt. 4.35 lbs. Each kit includes five individually packages [tuna, onions, limu (ogo seeweed), wet sauce mix, and dry sauce mix]. Each bulk kit is labeled with Costco item #13355. Costco deli department would upack the kit, mix all five components, repack, and sell at at Costco warehouse stores.
Why the product was recalled
Limu Poke (seaweed tuna) is recalled due to a potential for contamination with Salmonella. This product contains affected seaweed (Kahuku Ogo) which was recalled by Marine Agrifuture, LLC.
Distribution information
Alaska, Arizona, California, Colorado, Idaho, Illinois, Kansas, Louisiana, Michigan, Montana, Nebraska, Nevada, New Mexico, Ohio, Oregon, Texas, Utah, and Washington.
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: Telephone.
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.