Gorton's, Inc. Recall: May contain large and/or sharp fish bones - F-1070-2022

United States

TerminatedClass II

Company: Gorton's, Inc.
Product: Gorton s Fish Sandwich Fillets, 18.3 OZ, UPC 44400 15440
Recall date: April 26, 2022
Terminated: July 29, 2022
Source: FDA

Reason for recall

May contain large and/or sharp fish bones

April 26, 2022 - Recall initiated
May 25, 2022 - Reported by source
July 29, 2022 - Recall terminated

Recalled products
Product description	UPC	Quantity	Lot / code information
Gorton s Fish Sandwich Fillets, 18.3 OZ, UPC 44400 15440	Not published in this source record	350 Cases	DATE CODE: 2060F2 TIME RANGE: 15:30-17:30

Distribution

Official source record

Agency: FDA
Dataset: FDA Food Enforcement (Recalls)
Recall number: F-1070-2022
Event ID: 90090
Status: Terminated
Classification: Class II
Company: Gorton's, Inc.
Product description: Gorton s Fish Sandwich Fillets, 18.3 OZ, UPC 44400 15440
Quantity: 350 Cases
Reason: May contain large and/or sharp fish bones
Recall initiation date: April 26, 2022
Report date: May 25, 2022
Classification date: Not published in this source record
Termination date: July 29, 2022
Distribution pattern: NY, MA, PA, MD, VA, NC
UPC, lot, and code information: DATE CODE: 2060F2 TIME RANGE: 15:30-17:30
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: Gorton's, 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
New York	1
Massachusetts	1
Pennsylvania	1
Maryland	1
Virginia	1
North Carolina	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 II mean?

FDA classifies this recall as Class II. 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

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How to interpret this historical record

This record is preserved as published by FDA, as of July 29, 2022.

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

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