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RECALL RECORD — CLASS IIRecall closedF-0472-2021/FDA enforcement
Quirch Foods·Food·Mar 8, 2021

Yellowfin Tuna Portions Frozen Ivp-co Treated, NET WT 20 Lbs, Size 1 lb

What you need to know

Class II

  • What happened

    Fish decomposition and histamines

  • Health risk

    The product may cause temporary or medically reversible health consequences, or the probability of serious harm is remote. A safety issue that does not fit the standard pathogen, allergen, chemical or quality categories.

  • Action required

    Check the identifying codes below and stop using the product. Return it to the retailer for a refund or dispose of it safely, following the recall notice.

Recall closed · classified by the FDAPRMore food

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Product identification

Source: FDA FOOD

Brand nameQuirch Foods
Recalling firmQuirch FoodsCoral Gables, FL, United States
UPC / barcodesNo UPC listed in the FDA enforcement record.
Lot / date codes
  • Lot # 1413632, Best by Date: 9/7/2022
Distribution area
PR

Domestic distribution only-PR

United States

Quantity affected55 cases (20 X 1 lb per case)
Recall initiationFDA report date: April 28, 2021
FDA recall numberF-0472-2021

Beyond the headline

The recall, in context

Quirch Foods initiated this food recall on March 8, 2021. The FDA enforcement report states: Fish decomposition and histamines. The FDA report lists distribution as: Domestic distribution only-PR.

The FDA enforcement report describes the reason as: Fish decomposition and histamines

Yellowfin Tuna Portions Frozen Ivp-co Treated, NET WT 20 Lbs, Size 1 lb was made or distributed by Quirch Foods in Coral Gables, FL, United States. This page reflects FDA report F-0472-2021, dated April 28, 2021.

Why this is a Class II recall

Class II means the product may cause temporary or medically reversible health consequences, or the probability of serious harm is remote. In this recall, a safety issue that does not fit the standard pathogen, allergen, chemical or quality categories.

FDA definition

The product may cause temporary or medically reversible health consequences, or the probability of serious harm is remote.

What to do now

  1. 1

    Stop using it

    Do not eat, drink or take the affected product.

  2. 2

    Check the codes

    Compare the lot and date codes against the table above.

  3. 3

    Return or discard

    Contact the retailer or recalling firm about a refund, and dispose of the product safely.

Consumer safety guide

Undeclared fish

Symptoms to watch for

Hives, swelling, wheezing, vomiting or anaphylaxis can occur in people with a fish allergy.

When symptoms may appear

Reactions can begin within minutes to a few hours after eating the product.

Higher-risk groups

People with a diagnosed fish allergy, especially anyone with a history of anaphylaxis.

What to do now

  1. 1Do not eat the product if you have a fish allergy.
  2. 2Seek emergency care for breathing difficulty, throat swelling or other signs of anaphylaxis.
  3. 3Keep the packaging and contact the retailer or manufacturer about a refund.

This is general consumer safety information, not medical advice or a diagnosis. Follow the official recall notice and contact a healthcare professional if you have concerns about exposure or symptoms.

Frequently asked

Questions about this recall

What is the Yellowfin Tuna Portions Frozen Ivp-co Treated, NET WT 20 Lbs, Size 1 lb recall?

Quirch Foods recalled Yellowfin Tuna Portions Frozen Ivp-co Treated, NET WT 20 Lbs, Size 1 lb in an FDA Class II enforcement action reported as F-0472-2021. Fish decomposition and histamines

What should I do if I bought this product?

Check the identifying codes below and stop using the product. Return it to the retailer for a refund or dispose of it safely, following the recall notice. Do not eat the product if you have a fish allergy. Seek emergency care for breathing difficulty, throat swelling or other signs of anaphylaxis. Keep the packaging and contact the retailer or manufacturer about a refund.

Is the Quirch Foods recall still active?

The FDA lists this recall as recall closed. It remains relevant if you still have the affected product or need to identify a historical recall.

Where can I verify this recall?

This page is normalized from the openFDA enforcement record F-0472-2021. You can verify it directly using the official source link on this page. VerifyRecall updates its index from public FDA enforcement data and does not replace advice from the FDA, the recalling firm or a healthcare professional.

Verify before you act.

VerifyRecall is independent and not affiliated with the FDA. Always confirm the latest status on the official source record.

Official source

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Record last synced from official openFDA enforcement data on November 14, 2026. Source record: official FDA notice.