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Class I: serious health riskTerminated

Topway Enterprises Salmon Recall

Salmon (Cut)

Topway Enterprises, Inc · Houston, TX

Risk level
Class I
Reported by FDA
Jul 31, 2019
Recall ID
F-1992-2019
Check your lot numberHow we source this data

Summary

Topway Enterprises recalled Salmon starting Jul 3, 2019. The FDA classified it as Class I (serious health risk) and published enforcement report F-1992-2019 on Jul 31, 2019. Reason: Potential to be contaminated with Listeria monocytogenes. Status: Terminated.

Why it was recalled

Potential to be contaminated with Listeria monocytogenes.

Product description

Salmon (Cut)

Lot numbers, UPCs & expiration codes

None applied

Where it was sold

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

What to do if you have this product

  • Compare the brand, size, and lot/UPC codes on your package with the codes above.
  • If it matches, don't eat it. Return it to the store for a refund or throw it away.
  • Wash surfaces and containers that touched the product.
  • If you feel sick after eating it, contact your doctor. In an emergency call 911.

Recall details

Recall number
F-1992-2019
Classification
Class I
Status
Terminated
Recall initiated
Jul 3, 2019
FDA report date
Jul 31, 2019
Quantity
Approximately 8300 pounds
Recall type
Voluntary: Firm initiated
Recalling firm
Topway Enterprises, Inc

Original FDA data

Every field from FDA enforcement report F-1992-2019, exactly as published.

Show all FDA fields
City
Houston
State
TX
Status
Terminated
Country
United States
Event ID
83269
Address
4001 Briarpark Dr
Code information
None applied
Postal code
77042-5319
Report date
Jul 31, 2019
Product type
Food
Recall number
F-1992-2019
Classification
Class I
Recalling firm
Topway Enterprises, Inc
Product quantity
Approximately 8300 pounds
Termination date
Nov 21, 2019
Reason for recall
Potential to be contaminated with Listeria monocytogenes.
Voluntary / mandated
Voluntary: Firm initiated
Product description
Salmon (Cut)
Distribution pattern
distributed to Texas, Louisiana, Mississippi, Arkansas, Alabama, and the Gulf Coast area of Florida.
Recall initiation date
Jul 3, 2019
Initial firm notification
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Center classification date
Aug 12, 2019

How we source this data

Source: U.S. Food and Drug Administration enforcement report F-1992-2019, published Jul 31, 2019. View the source record (openFDA) · FDA enforcement reports

Last checked against FDA data: . Content last changed: .

FindMyRecall is an independent service and is not affiliated with or endorsed by the FDA. This page simplifies the official record; the FDA or manufacturer notice is authoritative, so follow its instructions.

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