Trident Item # 421048, Multi-Grain Alaskan Cod, Frozen, RETAIL packages, Net wt. 12 oz. UPC 0 28029 21048 4 The retail label is read in parts: "***Trident SEAFOODS***Multi-Grain Alaskan Cod***NET WT. 12 OZ.***". The retail case label is read in parts: "***Trident SEAFOODS***10 Grain Breaded Alaskan Cod***ITEM: 421048***12-12 oz. Cartons***NET WT. 9 lb.***KEEP FROZEN***".

Class I - Dangerous

What Should You Do?

  1. Check if you have this product:
    Lot Number A633511, Best By 11/30/2018 Lot Number A636225, Best By 12/27/2018
  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:
Trident Seafoods Corp - Island Enterprise M/V
Reason for Recall:
Multi-Grain Alaskan Cod, Frozen product, retail 12 oz. packages are recalled because they may contain small pieces of plastic.
Classification:
Class I - Dangerous

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

Status:
terminated

Product Information

Full Description:

Trident Item # 421048, Multi-Grain Alaskan Cod, Frozen, RETAIL packages, Net wt. 12 oz. UPC 0 28029 21048 4 The retail label is read in parts: "***Trident SEAFOODS***Multi-Grain Alaskan Cod***NET WT. 12 OZ.***". The retail case label is read in parts: "***Trident SEAFOODS***10 Grain Breaded Alaskan Cod***ITEM: 421048***12-12 oz. Cartons***NET WT. 9 lb.***KEEP FROZEN***".

Product Codes/Lot Numbers:

Lot Number A633511, Best By 11/30/2018 Lot Number A636225, Best By 12/27/2018

Distribution:

Nationwide distribution

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: F-2277-2017

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