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Food recall · FDA · Published August 11, 2020

Serafin Fishery recalls SERAFIN FISHERY Salmon Fish Dip, 8 oz

Serafin Fishery recalls 8 oz Salmon Fish Dip (lots 729 and 807) due to undeclared allergens including anchovies, eggs, milk, and soy. Consumers should avoid these products.

🇺🇸 FDA recall #F-1316-2020FoodSerafin Fishery ›
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Contact the company & request your remedy

Recalling firmSerafin Fishery2930 E Lapan Rd, N/A · Pinconning, MI 48650-9719
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

Serafin Fishery is recalling 8 oz Salmon Fish Dip products from specific lots because they contain undeclared allergens like anchovies, eggs, milk, and soy. This poses a risk for people with allergies to these ingredients. Read more at govinfonow.com/recall/15222-serafin-fishery-salmon-fish-dip-recall-undeclared-allergens.

Source Summary by GovInfoNow · govinfonow.com/recall/15222-serafin-fishery-salmon-fish-dip-recall-undeclared-allergens · Updated October 5, 2026 · FDA enforcement record: FDA #F-1316-2020

Cite this page

“Serafin Fishery Salmon Fish Dip Recall: Undeclared Allergens.” GovInfoNow, updated October 5, 2026. https://govinfonow.com/recall/15222-serafin-fishery-salmon-fish-dip-recall-undeclared-allergens. Based on FDA recall #F-1316-2020 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-1316-2020%22&limit=1).

Why it’s dangerous

The product contains undeclared allergens that could cause allergic reactions in people sensitive to anchovies, eggs, milk, or soy. These allergens were not listed on the product label, which is required by food safety regulations.

Who’s affected

People who have purchased the recalled Salmon Fish Dip products (lots 729 and 807) are at risk if they have allergies to anchovies, eggs, milk, or soy. Those with these allergies should avoid consuming the product.

How to tell if you have this one

Check for the product name 'Serafin Fishery Salmon Fish Dip, 8 oz' with lot numbers 729 or 807. The sell-by dates for these lots are August 12, 2020 and August 24, 2020.

  • Brand
    Serafin Fishery
  • Category
    Food
FDA recall event · 2 products

All 2 products in this recall

FDA lists each product line separately under one recall event. Check your product description, lot or code numbers against each row. Every row shares the hazard and remedy on this page.

  • Classification
    Class I
  • Status
    Terminated
  • Distribution
    locally in retail stores
Recall numberProduct, codes & lotsQuantity
F-1316-2020SERAFIN FISHERY Salmon Fish Dip, 8 oz; lot #729 and lot #807 Sell By dates of August 12, 2020 and August 24, 202090 units
F-1317-2020SERAFIN FISHERY Smoked Whitefish Dip, 8 oz; lot #729 and lot #807 Sell By dates of August 12, 2020 and August 24, 202085 units
Based on the official FDA remedy

What to do — step by step

  1. Check Product Lot Number

    Look for lot numbers 729 or 807 on the product label.

  2. Avoid Consuming Product

    Do not consume the recalled Salmon Fish Dip products if they have lot numbers 729 or 807.

✎ GovInfoNow

Questions people ask

What allergens are in the recalled product?

The recalled product contains undeclared allergens including anchovies, eggs, milk, and soy.

Which lots of Salmon Fish Dip are affected?

Lots 729 and 807 with sell-by dates of August 12, 2020 and August 24, 2020.

How can I check if I have the recalled product?

Check the product label for lot numbers 729 or 807 and sell-by dates of August 12, 2020 or August 24, 2020.

Take action

Contact Serafin Fishery

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

Subject: Recall F-1316-2020 — Serafin Fishery Serafin Fishery

Hello,

I own a Serafin Fishery that is covered by recall F-1316-2020 from Serafin Fishery.

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-1316-2020 (August 11, 2020) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-1316-2020 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