CLASS III Food recall · Reported 24 Sep 2025 · FDA Enforcement Report

Goldband Snapper Pristipomoides spp Fillets Skin-on Frozen, size recalled

E&E Foods is recalling Goldband Snapper Pristipomoides spp Fillets Skin-on Frozen, size 8, distributed in Colorado, Illinois, Minnesota, Missouri, Utah. The recall was initiated on 11 Sep 2025 and the FDA has classified it as Class III.

Check your package

Lot, batch or date codesProduction date: 21824, 21924, 22124, and 22224.
Quantity recalled925 cases

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

Recall details

Recall number
H-0620-2025
FDA event ID
97598
Recalling firm
E&E Foods, Renton, WA
Classification
Class III
Status
Terminated
Recall initiated
11 Sep 2025
FDA classified
22 Sep 2025
Reported
24 Sep 2025
Type
Voluntary: Firm initiated
Customers notified by
E-Mail
Reason category
Packaging Defects
Product category
Other

Timeline

11 Sep 2025Recall initiated by company
22 Sep 2025Classified by FDA+11 days
24 Sep 2025Published in enforcement report+2 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

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

Packaging recalls include wrong labels, wrong products in the wrong bottle, missing leaflets, short-filled or empty capsules and seals that fail.

Product as listed by the FDA

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.

Where it was distributed

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

ColoradoIllinoisMinnesotaMissouriUtah

Questions about this recall

Why was it recalled?

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

Which lots are affected?

Production date: 21824, 21924, 22124, and 22224.

Where was it sold?

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

What should I do if I have it?

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

What does Class III mean?

Class III recalls are for products unlikely to cause any adverse health consequence, usually labelling or quality issues.

Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

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