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Trident Seafoods Corp - Island Enterprise M/V Recall: Irregulars Battered Cod 3 oz Battered Diamonds is recalled because it may contain small pieces of plastic.
🇺🇸 United States
TerminatedClass II
Company
Trident Seafoods Corp - Island Enterprise M/V
Product
Trident Item # 474568, Irregulars Battered Cod 3 oz Battered…
Recall date
May 11, 2017
Terminated
April 2, 2018
Source
FDA
Reason for recall
Irregulars Battered Cod 3 oz Battered Diamonds is recalled because it may contain small pieces of plastic.
- Recall initiated
- Reported by source
- Recall terminated
Recalled products
Product description
UPC
Quantity
Lot / code information
Trident Item # 474568, Irregulars Battered Cod 3 oz Battered Diamonds, food service packages, frozen, Net wt. 10 lbs.
Not published in this source record
10 cases
Lot A631512. No best by date marked.
Distribution
distributed in AK
AL
AZ
CA
CO
IA
ID
IL
KS
LA
MA
MI
MN
MO
MS
NE
NJ
OH
OR
PA
SC
TN
TX
VT
WA
and WI.
Official source record
Agency
FDA
Dataset
FDA Food Enforcement (Recalls)
Recall number
F-2283-2017
Event ID
77246
Status
Terminated
Classification
Class II
Company
Trident Seafoods Corp - Island Enterprise M/V
Product description
Trident Item # 474568, Irregulars Battered Cod 3 oz Battered Diamonds, food service packages, frozen, Net wt. 10 lbs.
Quantity
10 cases
Reason
Irregulars Battered Cod 3 oz Battered Diamonds is recalled because it may contain small pieces of plastic.
Recall initiation date
May 11, 2017
Report date
June 7, 2017
Classification date
Not published in this source record
Termination date
April 2, 2018
Distribution pattern
distributed in AK, AL, AZ, CA, CO, IA, ID, IL, KS, LA, MA, MI, MN, MO, MS, NE, NJ, OH, OR, PA, SC, TN, TX, VT, WA, and WI.
UPC, lot, and code information
Lot A631512. No best by date marked.
Voluntary or mandated
Voluntary: Firm initiated
Initial notification method
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
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 77246 with 7 other product
entries in Public Health Trace.
FDA Recall🇺🇸 United StatesTerminatedHistorical recordClass II
A map highlighting the states named in the source's distribution description.
Distributed
No data published
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
Alaska
1
Alabama
1
Arizona
1
California
1
Colorado
1
Iowa
1
Idaho
1
Illinois
1
Kansas
1
Louisiana
1
Massachusetts
1
Michigan
1
Minnesota
1
Missouri
1
Mississippi
1
Nebraska
1
New Jersey
1
Ohio
1
Oregon
1
Pennsylvania
1
South Carolina
1
Tennessee
1
Texas
1
Vermont
1
Washington
1
Wisconsin
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.
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 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.
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or product is unsafe beyond what the official source has published.
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