Trident Seafoods Corporation Recall: Frozen non-ready to eat Alaskan Salmon Bites, Kroger brand, are recalled due to potential contamination with Listeria monocytogenes or Salmonella in vegetables ingredient.

🇺🇸 United States

1. October 18, 2018 - Recall initiated
2. November 14, 2018 - Reported by source
3. June 5, 2019 - Recall terminated

Official source record

Agency

FDA

Dataset

FDA Food Enforcement (Recalls)

Recall number

F-0424-2019

Event ID

81507

Status

Terminated

Classification

Class II

Company

Trident Seafoods Corporation

Product description

Kroger brand. Frozen non-ready to eat Alaskan Salmon Bites, Net Wt 12 oz (340 g). SKU # 83091. UPC on retail package: 0 11110 83091 3. UPC on master case: 1 00 11110 83091 0 The label is read in parts: "***Kroger ***multi-grain Breaded ALASKAN SALMON BITES ***COOKING INSTRUCTIONS***KEEP FROZEN UNTIL READY TO COOK***DISTRIBUTED BY THE KROGER CO. CINCINNATI, OHIO***".

Quantity

67,518 lbs.

Reason

Frozen non-ready to eat Alaskan Salmon Bites, Kroger brand, are recalled due to potential contamination with Listeria monocytogenes or Salmonella in vegetables ingredient.

Recall initiation date

October 18, 2018

Report date

November 14, 2018

Classification date

Not published in this source record

Termination date

June 5, 2019

Distribution pattern

Nationwide

UPC, lot, and code information

A731845. BEST BY: NOV 14 2019; A735141. BEST BY: DEC 15 2019; A800241. BEST BY: JAN 02 2020; A800342. BEST BY: JAN 02 2020; A804043. BEST BY: FEB 09 2020; A805743. BEST BY: FEB 09 2020; A806641. BEST BY: MAR 07 2020; A820551. BEST BY: MAR 07 2020; A822251. BEST BY: AUG 09 2020; A826951. BEST BY: SEP 25 2020; A827052. BEST BY: SEP 25 2020;

Voluntary or mandated

Voluntary: Firm initiated

Initial notification method

E-Mail

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: Trident Seafoods Corporation

Other recalls from Trident Seafoods Corporation

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.

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 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.

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