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 - Dangerous
Recalled: November 5, 2016 Western United Fish Company Seafood

What Should You Do?

  1. Check if you have this product:
    Packed on: November 3, 2016 and November 4, 2016. Use By: November 5, 2016 and November 6, 2016.
  2. Do not eat it: Even if it looks and smells fine, do not consume this product.
  3. Throw it away or return it: You can return the product to the store for a full refund.
  4. Seek medical attention if needed: If you've consumed this product and feel unwell, contact your doctor immediately.
  5. 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.gov

FDA Recall Number: F-0907-2017

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