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Topway Enterprises, Inc Recall: Potential to be contaminated with Listeria monocytogenes.

United States

TerminatedClass I

Company
Topway Enterprises, Inc
Product
Yellowfin Tuna
Recall date
July 3, 2019
Terminated
November 21, 2019
Source
FDA

Reason for recall

Potential to be contaminated with Listeria monocytogenes.

  1. - Recall initiated
  2. - Reported by source
  3. - Recall terminated
Recalled products
Product description UPC Quantity Lot / code information
Yellowfin Tuna Not published in this source record Approximately 3100 pounds None applied

Distribution

  • distributed to Texas
  • Louisiana
  • Mississippi
  • Arkansas
  • Alabama
  • and the Gulf Coast area of Florida.

Official source record

Agency
FDA
Dataset
FDA Food Enforcement (Recalls)
Recall number
F-1993-2019
Event ID
83269
Status
Terminated
Classification
Class I
Company
Topway Enterprises, Inc
Product description
Yellowfin Tuna
Quantity
Approximately 3100 pounds
Reason
Potential to be contaminated with Listeria monocytogenes.
Recall initiation date
July 3, 2019
Report date
July 31, 2019
Classification date
Not published in this source record
Termination date
November 21, 2019
Distribution pattern
distributed to Texas, Louisiana, Mississippi, Arkansas, Alabama, and the Gulf Coast area of Florida.
UPC, lot, and code information
None applied
Voluntary or mandated
Voluntary: Firm initiated
Initial notification method
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Source last updated
Not tracked separately from the Public Health Trace retrieval date below
Public Health Trace retrieval date

Other products recalled under this same event

This recall shares FDA event ID 83269 with 1 other product entry in Public Health Trace.

FDA Recall United States Terminated Historical recordClass I

Topway Enterprises, Inc

Product
Salmon (Cut)
Published
July 31, 2019
Distribution
distributed to Texas, Louisiana, Mississ…

View recall →

Responsible company: Topway Enterprises, Inc

Other recalls from Topway Enterprises, Inc

FDA Recall United States Terminated Historical recordClass II

Topway Enterprises, Inc

Product
Tuna cut and packaged in Styrofoam case approximately 19 kg…
Published
August 12, 2020
Distribution
TX, Louisiana, Mississippi, Florida, Ten…

View recall →

FDA Recall United States Terminated Historical recordClass II

Topway Enterprises, Inc

Product
Salmon cut and packaged in Styrofoam case approximately 19 k…
Published
August 12, 2020
Distribution
TX, Louisiana, Mississippi, Florida, Ten…

View recall →

FDA Recall United States Terminated Historical recordClass I

Topway Enterprises, Inc

Product
Salmon (Cut)
Published
July 31, 2019
Distribution
distributed to Texas, Louisiana, Mississ…

View recall →

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 I mean?

A situation in which there is a reasonable probability that use of or exposure to a product will cause serious adverse health consequences or death.

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.