CLASS II Food recall · Reported 4 Mar 2015 · FDA Enforcement Report
Pacific Fusion Frozen Tuna Steak Wild Caught recalled
Thai Ocean Venture is recalling Pacific Fusion Frozen Tuna Steak Wild Caught, distributed in Washington. The recall was initiated on 15 Dec 2014 and the FDA has classified it as Class II.
Check your package
Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.
Recall details
- Recall number
- F-0801-2015
- FDA event ID
- 70047
- Recalling firm
- Thai Ocean Venture, Muang Phuket, N/A
- Brand
- Pacific Fusion
- Classification
- Class II
- Status
- Terminated
- Recall initiated
- 15 Dec 2014
- FDA classified
- 25 Feb 2015
- Reported
- 4 Mar 2015
- Type
- Voluntary: Firm initiated
- Customers notified by
- Reason category
- Packaging Defects
- Product category
- Beef
Timeline
| 15 Dec 2014 | Recall initiated by company | |
| 25 Feb 2015 | Classified by FDA | +72 days |
| 4 Mar 2015 | Published in enforcement report | +7 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
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.
Packaging recalls include wrong labels, wrong products in the wrong bottle, missing leaflets, short-filled or empty capsules and seals that fail.
Product as listed by the FDA
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).
Where it was distributed
Product was distributed to three distributors located within the U.S. (WA and OR).
Questions about this recall
Why was it 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.
Which lots are affected?
SKU: 0 75627 14610 3 Production Date: 10 MAR 2014 Best Before: 10 MAR 2016
Where was it sold?
Product was distributed to three distributors located within the U.S. (WA and OR).
What should I do if I have it?
Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.
What does Class II mean?
Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.
Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.