FDA recall record

Thai Ocean Venture Co Pacific Fusion Frozen Tuna Steak Wild Caught Net Weight: 15 lb recall — FDA F-0801-2015

The firm initiated a recall as a result of a consumer complaint being received and samples collected by the FDA being found with high levels of histamine.

Class IIclassification
F-0801-2015official record ID
Mar 4, 2015report date

Recall record at a glance

Official recordF-0801-2015
CategoryFood Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmThai Ocean Venture Co., Ltd.
Report dateMar 4, 2015
Recall initiation dateDec 15, 2014
Quantity690 cases (17-19 pieces per master carton)
LocationMuang Phuket, N/A, Thailand

Official product description

Pacific Fusion Frozen Tuna Steak Wild Caught Net Weight: 15 lb (240oz) 6.80 kg Ingredients: Tuna, tasteless smoke used as a preservative to promote color retention SKU: 0 75627 14610 3 Production Date: 10 MAR 2014 Best Before: 10 MAR 2016 Manufactured By: Thai Ocean Venture Co. 64/213 moo 7, Anupas phuketkan Rd. Rassada Muang, Pukey Thailand Imported By: Gourmet Fusion Food, INc. 5730 Uplander Way Ste. 110 Culver City CA 90230 Product of Thailand Wild Caught Product is raw, frozen and packaged in reduced oxygen packaging (ROP).

Why the product was recalled

The firm initiated a recall as a result of a consumer complaint being received and samples collected by the FDA being found with high levels of histamine.

Distribution information

Product was distributed to three distributors located within the U.S. (WA and OR).

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: E-Mail.

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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