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Taiwan Seafood & Fish Corporation Recall: Taiwan Seafood & Fish Corp initiated a recall of the ground Yellowfin tuna due to high levels of histamine.

United States

TerminatedClass II

Company
Taiwan Seafood & Fish Corporation
Product
Yellowfin Tuna Ground Meat, 22 lbs./case, 5500 lbs Two bo…
Recall date
October 3, 2016
Terminated
December 8, 2016
Source
FDA

Reason for recall

Taiwan Seafood & Fish Corp initiated a recall of the ground Yellowfin tuna due to high levels of histamine.

  1. - Recall initiated
  2. - Reported by source
  3. - Recall terminated
Recalled products
Product description UPC Quantity Lot / code information
Yellowfin Tuna Ground Meat, 22 lbs./case, 5500 lbs Two boxes per case, 11 one pound packages per box, 22 one pound packages per case Not published in this source record 250 cases (5500 lbs.) 6037

Distribution

  • US: NY
  • CA
  • MA

Official source record

Agency
FDA
Dataset
FDA Food Enforcement (Recalls)
Recall number
F-0678-2017
Event ID
75797
Status
Terminated
Classification
Class II
Company
Taiwan Seafood & Fish Corporation
Product description
Yellowfin Tuna Ground Meat, 22 lbs./case, 5500 lbs Two boxes per case, 11 one pound packages per box, 22 one pound packages per case
Quantity
250 cases (5500 lbs.)
Reason
Taiwan Seafood & Fish Corp initiated a recall of the ground Yellowfin tuna due to high levels of histamine.
Recall initiation date
October 3, 2016
Report date
December 14, 2016
Classification date
Not published in this source record
Termination date
December 8, 2016
Distribution pattern
US: NY, CA, MA,
UPC, lot, and code information
6037
Voluntary or mandated
Voluntary: Firm initiated
Initial notification method
Telephone
Source last updated
Not tracked separately from the Public Health Trace retrieval date below
Public Health Trace retrieval date

Responsible company: Taiwan Seafood & Fish Corporation

Distribution map

A map highlighting the states named in the source's distribution description.

Shading reflects state-level totals only, as published by the source. It does not imply county-level or point-level precision.

Distribution map
State Distributed
New York 1
California 1
Massachusetts 1

States shown are extracted from the source's free-text distribution description above; a narrative description (e.g. "distributed nationwide") may not list individual states to extract.

Where this information comes from

View FDA enforcement record -- the specific openFDA record this summary was built from.

No separate FDA public notice was found for this enforcement record. The information below comes from FDA's Recall Enterprise System through openFDA.

FDA Enforcement Reports -- FDA's general, official recall and enforcement information.

Technical source data

View raw source data -- the machine-readable record this page's information was built from.

Retrieved by Public Health Trace:

Frequently asked questions

What does a Class II mean?

A situation in which use of or exposure to a product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote.

Is this recall still active?

According to FDA, this recall's status is "Terminated." Always confirm the current status using the source links below, since status can change after Public Health Trace last retrieved this record.

What should I do if I have this product?

Follow the instructions published by the responsible agency (see the source links below) -- recall guidance (e.g. dispose of the product, return it for a refund, or check for a specific lot number) varies by recall and is set by that agency, not by Public Health Trace.

Where can I find more official information?

The source links below, published by FDA, are the authoritative record for this recall, including any updates issued after this summary was retrieved.

This summary is based on the official source record referenced above. Public Health Trace does not state that any company or product is unsafe beyond what the official source has published. Read the full medical disclaimer.