Approximately 5 lb bag of Pre-cooked Conch Fritters labeled in part: "***NEPTUNE'S CONCH FRITTERS PRECOOKED***Ingredients: Conch, Flour, Onions, Milk, Bell Peppers, Eggs, Garlic, Salt, Black Pepper, Lime Juice & Hot Pepper Sauce.***Packed by Triton Seafood Co. Miami, FL 33166***Pack: 125 Units Net Wt. 5# (approx.)***

Class I - Dangerous
Recalled: April 28, 2011 Triton Seafood Dairy & Eggs

What Should You Do?

  1. Check if you have this product:
    W152BA, W152BB, W153BC, W152BD, W152BE, W162BA, W162BB, W162BC, W162BD, W162BE, W172BA, W172BB, W172BC, W172DB
  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:
Triton Seafood Co.
Reason for Recall:
Triton Seafood Co recalled their Neptune brand frozen Pre-cooked Conch Fritters and Conch Fritter Batter because the allergen, "Wheat" was not identified on the product label.
Classification:
Class I - Dangerous

Dangerous or defective products that predictably could cause serious health problems or death.

Status:
terminated

Product Information

Full Description:

Approximately 5 lb bag of Pre-cooked Conch Fritters labeled in part: "***NEPTUNE'S CONCH FRITTERS PRECOOKED***Ingredients: Conch, Flour, Onions, Milk, Bell Peppers, Eggs, Garlic, Salt, Black Pepper, Lime Juice & Hot Pepper Sauce.***Packed by Triton Seafood Co. Miami, FL 33166***Pack: 125 Units Net Wt. 5# (approx.)***

Product Codes/Lot Numbers:

W152BA, W152BB, W153BC, W152BD, W152BE, W162BA, W162BB, W162BC, W162BD, W162BE, W172BA, W172BB, W172BC, W172DB

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: F-2376-2012

Related Recalls