FDA recall record

Michael's Seafood Inc. DBA Michael's Gourmet & Alaskan Wild Smoked Sockeye Salmon in vacuum recall — FDA 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…

Class Iclassification
F-0866-2013official record ID
Jan 16, 2013report date

Recall record at a glance

Official recordF-0866-2013
CategoryFood Recalls
ClassificationClass I
FDA record statusTerminated
Recalling firmMichael's Seafood Inc. DBA Michael's Gourmet & Delicacies
Report dateJan 16, 2013
Recall initiation dateOct 27, 2012
Quantity2,440 pieces and 250 lbs. of Trimmings
LocationMiami, FL, United States

Official product description

Alaskan Wild Smoked Sockeye Salmon in vacuum packed plastic package, labeled in part: "MICHAEL'S WILD SOCKEYE SMOKED SALMON***INGREDIENTS: WILD ALASKAN SOCKEYE SALMON, SALT, SUGAR, NATURAL HARDWOOD SMOKE.***KEEP FROZEN UNTIL USE/THAWED UNDER REFRIGERATION IMMEDIATELY BEFORE USE.***DISTRIBUTED BY: MICHAEL'S SEAFOOD INC. 500 NE 185TH STREET, MIAMI FL 33179.***"READY TO EAT WITHIN 3 DAYS AFTER OPENING OR BEFORE SELL BY DATE.***"

Why the product was recalled

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.

Distribution information

Products was distributed in Florida.

How to read the classification

FDA Class I indicates a situation in which there is a reasonable probability that use of or exposure to the product will cause serious adverse health consequences or death. The classification shown here comes directly from the FDA enforcement record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

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