FDA recall record

ALFA INTERNATIONAL SEAFOOD Fl, 8402, Yellowfin Tuna Loins, Previously Frozen, Wild recall — FDA F-2245-2019

Alfa International Seafood Inc. was notified by Kroger retail stores of complaints from consumers who experienced symptoms of scombroid poisoning after…

Class IIclassification
F-2245-2019official record ID
Oct 2, 2019report date

Recall record at a glance

Official recordF-2245-2019
CategoryFood Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmALFA INTERNATIONAL SEAFOOD Inc.
Report dateOct 2, 2019
Recall initiation dateSep 6, 2019
Quantity8,585.99 pounds
LocationMedley, FL, United States

Official product description

Alfa International Seafood Miami, Fl, 8402, Yellowfin Tuna Loins, Previously Frozen, Wild Caught, Product of Vietnam

Why the product was recalled

Alfa International Seafood Inc. was notified by Kroger retail stores of complaints from consumers who experienced symptoms of scombroid poisoning after eating yellowfin tuna steaks supplied by Alfa International Seafood Inc.

Distribution information

Domestic distribution

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA 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.

About this record

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