FDA recall record

SUSHI HOUSE Frozen Raw Yellowfin Tuna Ground Meat recall — FDA F-0574-2015

Sushi House Inc. is conducting a voluntary recall of Heartlight Ground Tuna because it may contain histamines which exceed 50 ppm.

Class IIclassification
F-0574-2015official record ID
Dec 3, 2014report date

Recall record at a glance

Official recordF-0574-2015
CategoryFood Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmSUSHI HOUSE Inc.
Report dateDec 3, 2014
Recall initiation dateNov 5, 2014
Quantity280 boxes
LocationPalisades Park, NJ, United States

Official product description

Frozen Raw Yellowfin Tuna Ground Meat (Thunnus albacares), Grade: AAA, Net Weight: 10 lbs (100%), Wild Caught, Product of Indonesia, Imported and distributed by Heartlight Seafood LLC, 429 SW 195th Ave., Pembroke Pines, FL 33029, Production Date: 06/10/2014, Best used by 06/10/2016, UPC 207935110006

Why the product was recalled

Sushi House Inc. is conducting a voluntary recall of Heartlight Ground Tuna because it may contain histamines which exceed 50 ppm.

Distribution information

CT, NJ and NY

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: Telephone.

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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