RECALL RECORD — CLASS IRecall closedF-0866-2013/FDA enforcement

Alaskan Wild Smoked Sockeye Salmon in Vacuum Packed Plastic Package, Labeled in Part: &Amp

What you need to know

Class I
  • What happened

    Michael's Gourmet Delicacies, Miami, FL is recalling their Alaskan Wild Smoked Sockeye Salmon, Batch #1443 (4oz., 8 oz., 16 oz. and Trimmings) after a sample of 4 oz. Smoked…

  • Health risk

    The product has a reasonable probability of causing serious adverse health consequences or death. A hardy bacteria that can grow at refrigerator temperatures and cause severe illness in vulnerable groups.

  • Action required

    Do not eat the product. Check the lot and UPC codes below, then discard it or return it to the retailer for a refund. If you have already eaten it, monitor for symptoms and seek medical care if they are severe or persistent.

Recall closed · classified by the FDAINMore food

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Product identification

Source: FDA FOOD

Brand nameMichael's Seafood INC. Dba Michael's Gourmet & Delicacies
Recalling firmMichael's Seafood INC. Dba Michael's Gourmet & DelicaciesMiami, FL, United States
UPC / barcodesNo UPC listed in the FDA enforcement record.
Lot / date codes
  • Batch #1443
Distribution area
IN

Products was distributed in Florida.

United States

Quantity affected2, 440 pieces and 250 lbs. of Trimmings
Recall initiationFDA report date: January 16, 2013
FDA recall numberF-0866-2013

Beyond the headline

The recall, in context

Michael's Seafood INC. Dba Michael's Gourmet & Delicacies initiated this food recall on October 27, 2012. The FDA enforcement report states: Michael's Gourmet Delicacies, Miami, FL is recalling their Alaskan Wild Smoked Sockeye Salmon, Batch #1443 (4oz., 8 oz., 16 oz. and Trimmings) after a sample of 4 oz. Smoked Sockeye Salmon tested positive for Listeria Monocytogenes. The FDA report lists distribution as: Products was distributed in Florida.

The FDA enforcement report describes the reason as: Michael's Gourmet Delicacies, Miami, FL is recalling their Alaskan Wild Smoked Sockeye Salmon, Batch #1443 (4oz., 8 oz., 16 oz. and Trimmings) after a sample of 4 oz. Smoked Sockeye Salmon tested positive for Listeria Monocytogenes.

Alaskan Wild Smoked Sockeye Salmon in Vacuum Packed Plastic Package, Labeled in Part: &Amp was made or distributed by Michael's Seafood INC. Dba Michael's Gourmet & Delicacies in Miami, FL, United States. This page reflects FDA report F-0866-2013, dated January 16, 2013.

Why this is a Class I recall

Class I means the product has a reasonable probability of causing serious adverse health consequences or death. In this recall, a hardy bacteria that can grow at refrigerator temperatures and cause severe illness in vulnerable groups.

FDA definition

The product has a reasonable probability of causing serious adverse health consequences or death.

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

Listeria monocytogenes

Symptoms to watch for

Fever, muscle aches, nausea and diarrhea may occur. Severe infection can cause headache, stiff neck, confusion, loss of balance or convulsions.

When symptoms may appear

Symptoms can begin within a few days, but can take up to several weeks to appear.

Higher-risk groups

Pregnant people, newborns, adults over 65 and immunocompromised people are at the highest risk of severe illness.

What to do now

  1. 1Stop using or eating the affected product and keep it away from children and pets.
  2. 2Match the product against the UPC and lot/date codes on this page, then dispose of it safely or return it to the retailer.
  3. 3If you have already been exposed and develop severe or worsening symptoms, seek medical advice promptly.

General guidance based on CDC and FDA consumer information.

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 Alaskan Wild Smoked Sockeye Salmon in Vacuum Packed Plastic Package, Labeled in Part: &Amp recall?

Michael's Seafood INC. Dba Michael's Gourmet & Delicacies recalled Alaskan Wild Smoked Sockeye Salmon in Vacuum Packed Plastic Package, Labeled in Part: &Amp in an FDA Class I enforcement action reported as F-0866-2013. Michael's Gourmet Delicacies, Miami, FL is recalling their Alaskan Wild Smoked Sockeye Salmon, Batch #1443 (4oz., 8 oz., 16 oz. and Trimmings) after a sample of 4 oz. Smoked…

What should I do if I bought this product?

Do not eat the product. Check the lot and UPC codes below, then discard it or return it to the retailer for a refund. If you have already eaten it, monitor for symptoms and seek medical care if they are severe or persistent. Stop using or eating the affected product and keep it away from children and pets. Match the product against the UPC and lot/date codes on this page, then dispose of it safely or return it to the retailer. If you have already been exposed and develop severe or worsening symptoms, seek medical advice promptly.

Is the Michael's Seafood INC. Dba Michael's Gourmet & Delicacies 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-0866-2013. 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.