Goldband Snapper Pristipomoides spp Fillets Skin-on Frozen, size 8-10oz, , item #991900011, individually Vacuum Package
Summary
The FDA issued a Class III for Goldband Snapper Pristipomoides spp Fillets Skin-on Frozen, size 8-10oz, , item by E&E Foods Inc. Reason: Goldband Snapper is recalled because testing confirmed fish is Sharptooth Snapper..
Details
Source
Food Recall
External ID
H-0620-2025
Action Date
2025-09-24
Status
Terminated
Category
food
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.
Lot/Code Info: Production date: 21824, 21924, 22124, and 22224.
Quantity Affected: 925 cases
Reason for Recall
Goldband Snapper is recalled because testing confirmed fish is Sharptooth Snapper.
Distribution
Distributed in CO, IL, MO, MN and UT.
Type: Voluntary: Firm initiated
Recall Initiated: 2025-09-11
Company
Renton, WA
Context & Analysis
This is a Class III recall. Class III recalls involve products unlikely to cause adverse health consequences, but that violate FDA regulations.
This was one of 51 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Frequently Asked Questions
What is a Class III recall?
A Class III recall involves products that are unlikely to cause adverse health effects but violate FDA labeling or manufacturing regulations.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (E&E Foods Inc) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does E&E Foods Inc have FDA actions?
This is the only FDA action we have on record for E&E Foods Inc in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "H-0620-2025" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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