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.
Class I - DangerousWhat Should You Do?
- Check if you have this product: Packed on: November 3, 2016 and November 4, 2016. Use By: November 5, 2016 and November 6, 2016.
- Do not eat it: Even if it looks and smells fine, do not consume this product.
- Throw it away or return it: You can return the product to the store for a full refund.
- Seek medical attention if needed: If you've consumed this product and feel unwell, contact your doctor immediately.
- Report problems: Report any issues to the FDA's Safety Reporting Portal.
⚠️ Emergency: If you experience severe symptoms after consuming this product, call 911 or Poison Control at 1-800-222-1222.
Recall Details
- Company:
- Western United Fish Company, Inc.
- Reason for Recall:
- 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.
- Classification:
- Class I - Dangerous
Dangerous or defective products that predictably could cause serious health problems or death.
- Status:
- terminated
Product Information
Full 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.
Product Codes/Lot Numbers:
Packed on: November 3, 2016 and November 4, 2016. Use By: November 5, 2016 and November 6, 2016.
Official Source
Always verify recall information with the official FDA source:
View on FDA.govFDA Recall Number: F-0907-2017
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