Jensen Tuna Inc Recall: Potential to be contaminated with Salmonella. - F-1343-2019

United States

TerminatedClass I

Company: Jensen Tuna Inc
Product: Frozen ground tuna, 1 lb package, 20 packages/case
Recall date: April 15, 2019
Terminated: June 23, 2020
Source: FDA

Reason for recall

Potential to be contaminated with Salmonella.

April 15, 2019 - Recall initiated
May 22, 2019 - Reported by source
June 23, 2020 - Recall terminated

Recalled products
Product description	UPC	Quantity	Lot / code information
Frozen ground tuna, 1 lb package, 20 packages/case	Not published in this source record	46,336 lbs	Lot codes Z266, Z271, Z272

Distribution

Official source record

Agency: FDA
Dataset: FDA Food Enforcement (Recalls)
Recall number: F-1343-2019
Event ID: 82628
Status: Terminated
Classification: Class I
Company: Jensen Tuna Inc
Product description: Frozen ground tuna, 1 lb package, 20 packages/case
Quantity: 46,336 lbs
Reason: Potential to be contaminated with Salmonella.
Recall initiation date: April 15, 2019
Report date: May 22, 2019
Classification date: Not published in this source record
Termination date: June 23, 2020
Distribution pattern: MD, FL, LA, IL, CA, WA, NY, MN, AZ, TX
UPC, lot, and code information: Lot codes Z266, Z271, Z272
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: July 18, 2026 ET

Responsible company: Jensen Tuna Inc

Distribution map

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
Maryland	1
Florida	1
Louisiana	1
Illinois	1
California	1
Washington	1
New York	1
Minnesota	1
Arizona	1
Texas	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.

This record comes from FDA's Enforcement Report database. Not every Enforcement Report record has a separate FDA.gov recall-announcement page.

FDA Enforcement Reports -- FDA's general, official recall and enforcement information. See FDA Enforcement Reports versus recall announcements for how that database differs from a press-release-style announcement.

New to reading a recall record? See how to read an FDA recall record and what recall statuses mean.

Technical source data

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

Retrieved by Public Health Trace: July 18, 2026 ET

Frequently asked questions

What does a Class I mean?

FDA classifies this recall as Class I. See how to read an FDA recall record (linked above) for what each classification level means.

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 responsible agency's published instructions, linked below -- recall guidance is set by that agency, not by Public Health Trace.

Official guidance and record verification

Public Health Trace does not provide medical advice -- review the linked official source below for current, authoritative information.

How to interpret this historical record

This record is preserved as published by FDA, as of June 23, 2020.

Status as reported: Terminated.

This page does not imply a current danger or a current consumer instruction -- review the official source for the most current information.

View the official FDA source

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.