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Food recall · FDA · Published June 18, 2020

Trident Seafoods Corporation recalls Gordon Choice Imitation Crab Supreme Style, Net Wt 40 oz (2 lb 8 oz) Keep Frozen. UPC 93901-71212. For Distribution

Trident Seafoods recalls Gordon Choice Imitation Crab Supreme Style (40 oz) due to possible undeclared egg white. Products produced before June 18, 2020, with specific lot codes are affected. Consumers should check packaging for lot codes and expiration dates.

🇺🇸 FDA recall #F-1019-2020FoodTrident Seafoods ›
Take action

Contact the company & request your remedy

Recalling firmTrident Seafoods Corporation5303 Shilshole Ave Nw, N/A · Seattle, WA 98107-4021
No email on file for this recall — reach the company by phone or its official page instead.No email on file — write to the address above instead.
✎ GovInfoNow plain-language explainer

What happened, in plain English

Trident Seafoods is recalling Gordon Choice Imitation Crab Supreme Style products that may contain undeclared egg white. This could pose a risk for people with egg allergies who might react to the egg white. Read more at govinfonow.com/recall/15692-gordon-choice-imitation-crab-supreme-undeclared-egg-white-recall.

Source Summary by GovInfoNow · govinfonow.com/recall/15692-gordon-choice-imitation-crab-supreme-undeclared-egg-white-recall · Updated October 5, 2026 · FDA enforcement record: FDA #F-1019-2020

Cite this page

“Gordon Choice Imitation Crab Supreme: Undeclared Egg White Recall.” GovInfoNow, updated October 5, 2026. https://govinfonow.com/recall/15692-gordon-choice-imitation-crab-supreme-undeclared-egg-white-recall. Based on FDA recall #F-1019-2020 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-1019-2020%22&limit=1).

Why it’s dangerous

The product may contain undeclared egg white, which could cause allergic reactions in people sensitive to eggs. This is a food safety issue related to ingredient labeling.

Who’s affected

People who purchased Gordon Choice Imitation Crab Supreme Style products with lot codes M828803 through M016004, produced before June 18, 2020, are affected. Those with egg allergies are at higher risk due to potential undeclared egg white.

How to tell if you have this one

Check the product packaging for lot codes: M828803 (expires 10/15/2020), M904202 (expires 02/11/2021), M916303 (expires 06/12/2021), M935004 (expires 12/16/2021), or M016004 (expires 06/08/2022). Products were produced before June 18, 2020.

  • Brand
    Trident Seafoods
  • Product
    Gordon Choice Imitation Crab Supreme Style, Net Wt 40 oz (2 lb 8 oz) Keep Frozen. UPC 93901-71212. For Distribution
  • Category
    Food
Based on the official FDA remedy

What to do — step by step

  1. Check Product Packaging

    Look for lot codes on the packaging: M828803, M904202, M916303, M935004, or M016004.

✎ GovInfoNow

Questions people ask

What products are affected by this recall?

Gordon Choice Imitation Crab Supreme Style products with lot codes M828803 through M016004, produced before June 18, 2020.

Why is this product being recalled?

The product may contain undeclared egg white, which could cause allergic reactions in people sensitive to eggs.

How do I know if I have the recalled product?

Check the product packaging for lot codes: M828803 (expires 10/15/2020), M904202 (expires 02/11/2021), M916303 (expires 06/12/2021), M935004 (expires 12/16/2021), or M016004 (expires 06/08/2022).

Take action

Contact Trident Seafoods

We’ve drafted a message you can send Trident Seafoods to request your refund or repair — edit it as you like.

Subject: Recall F-1019-2020 — Trident Seafoods Gordon Choice Imitation Crab Supreme Style, Net Wt 40 oz (2 lb 8 oz) Keep Frozen. 

Hello,

I own a Gordon Choice Imitation Crab Supreme Style, Net Wt 40 oz (2 lb 8 oz) Keep Frozen. UPC 93901-71212. For Distribution that is covered by recall F-1019-2020 from Trident Seafoods.

I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this?

Thank you.

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Where this comes from

The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.

  • Official source: FDA Recall #F-1019-2020 (June 18, 2020) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-1019-2020 to see it in context.
  • Plain-language summary written by qwen3:4b on October 5, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
  • GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.
GovInfoNow is an independent guide. We are not FDA or any government agency. Always confirm details with the official recall.Data: CPSC · FDA · NHTSA · USDA