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RELISH FOODS, INC. Recall: Salmonella found in FDA samples of tuna loins.

United States

TerminatedClass I

Company
RELISH FOODS, INC.
Product
Newport -Yellowfin Tuna Loin; (3/5 lbs. and 5/8 lbs.) Froze…
Recall date
October 16, 2017
Terminated
November 6, 2019
Source
FDA

Reason for recall

Salmonella found in FDA samples of tuna loins.

  1. - Recall initiated
  2. - Reported by source
  3. - Recall terminated
Recalled products
Product description UPC Quantity Lot / code information
Newport -Yellowfin Tuna Loin; (3/5 lbs. and 5/8 lbs.) Frozen, packed in 30 lb. (480 oz.) 13.61 KG cardboard box. Product of Indonesia. Ingredients: Yellowfin tuna (fish), Water, carbon monoxide (for color retention). Not published in this source record 1,966 Cases Lot Nos. MTNT 0947C, MTNT 0957B, MTNT 0967A, MTNT 0977D MTNT 0917B, MTNT 0937D, GND 0737D, GND 0747E, GND 0757A, GND 0767C, GND 0777B

Distribution

  • U.S. distribution to the following: OR
  • WA
  • CA
  • AZ
  • ID
  • MT
  • NV
  • UT
  • WY
  • CO. No foreign distribution.

Official source record

Agency
FDA
Dataset
FDA Food Enforcement (Recalls)
Recall number
F-0110-2018
Event ID
78324
Status
Terminated
Classification
Class I
Company
RELISH FOODS, INC.
Product description
Newport -Yellowfin Tuna Loin; (3/5 lbs. and 5/8 lbs.) Frozen, packed in 30 lb. (480 oz.) 13.61 KG cardboard box. Product of Indonesia. Ingredients: Yellowfin tuna (fish), Water, carbon monoxide (for color retention).
Quantity
1,966 Cases
Reason
Salmonella found in FDA samples of tuna loins.
Recall initiation date
October 16, 2017
Report date
November 8, 2017
Classification date
Not published in this source record
Termination date
November 6, 2019
Distribution pattern
U.S. distribution to the following: OR, WA, CA, AZ, ID, MT, NV, UT, WY, CO. No foreign distribution.
UPC, lot, and code information
Lot Nos. MTNT 0947C, MTNT 0957B, MTNT 0967A, MTNT 0977D MTNT 0917B, MTNT 0937D, GND 0737D, GND 0747E, GND 0757A, GND 0767C, GND 0777B
Voluntary or mandated
Voluntary: Firm initiated
Initial notification method
Letter
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 78324 with 1 other product entry in Public Health Trace.

FDA Recall United States Terminated Historical recordClass I

RELISH FOODS, INC.

Product
Newport -Yellowfin Tuna Steaks; (4 oz. and 6 oz.) Frozen, p…
Published
November 8, 2017
Distribution
U.S. distribution to the following: OR,…

View recall →

Responsible company: RELISH FOODS, INC.

Other recalls from RELISH FOODS, INC.

FDA Recall United States Terminated Historical recordClass I

RELISH FOODS, INC.

Product
Newport -Yellowfin Tuna Steaks; (4 oz. and 6 oz.) Frozen, p…
Published
November 8, 2017
Distribution
U.S. distribution to the following: OR,…

View recall →

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
Oregon 1
Washington 1
California 1
Arizona 1
Idaho 1
Montana 1
Nevada 1
Utah 1
Wyoming 1
Colorado 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 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.