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E&E Foods Inc Recall: Goldband Snapper is recalled because testing confirmed fish is Sharptooth Snapper.

United States

TerminatedClass III

Company
E&E Foods Inc
Product
Goldband Snapper Pristipomoides spp Fillets Skin-on Frozen,…
Recall date
September 11, 2025
Terminated
January 6, 2026
Source
FDA

Reason for recall

Goldband Snapper is recalled because testing confirmed fish is Sharptooth Snapper.

  1. - Recall initiated
  2. - Reported by source
  3. - Recall terminated
Recalled products
Product description UPC Quantity Lot / code information
Goldband Snapper Pristipomoides spp Fillets Skin-on Frozen, size 8-10oz, , item #991900011, individually Vacuum Package (IVP) portions in a plain white cardboard box, net wt. 10 lbs. per box. Product is wild caught, product of Indonesia, distributed by E&E Foods, Renton, WA. Not published in this source record 925 cases Production date: 21824, 21924, 22124, and 22224.

Distribution

  • Distributed in CO
  • IL
  • MO
  • MN and UT.

Official source record

Agency
FDA
Dataset
FDA Food Enforcement (Recalls)
Recall number
H-0620-2025
Event ID
97598
Status
Terminated
Classification
Class III
Company
E&E Foods Inc
Product description
Goldband Snapper Pristipomoides spp Fillets Skin-on Frozen, size 8-10oz, , item #991900011, individually Vacuum Package (IVP) portions in a plain white cardboard box, net wt. 10 lbs. per box. Product is wild caught, product of Indonesia, distributed by E&E Foods, Renton, WA.
Quantity
925 cases
Reason
Goldband Snapper is recalled because testing confirmed fish is Sharptooth Snapper.
Recall initiation date
September 11, 2025
Report date
September 24, 2025
Classification date
Not published in this source record
Termination date
January 6, 2026
Distribution pattern
Distributed in CO, IL, MO, MN and UT.
UPC, lot, and code information
Production date: 21824, 21924, 22124, and 22224.
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

Responsible company: E&E Foods Inc

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
Colorado 1
Illinois 1
Missouri 1
Minnesota 1
Utah 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 III mean?

A situation in which use of or exposure to a product is not likely to cause adverse health consequences.

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?

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