Class IIITerminatedVoluntary: Firm initiated
E&E Foods Inc: food recall H-0620-2025
E&E Foods Inc of Renton, WA recalled Goldband Snapper Pristipomoides spp Fillets Skin-on Frozen, size 8-10oz, , item #991900011, individually Vacuum… Reason: Goldband Snapper is recalled because testing confirmed fish is Sharptooth Snapper. The FDA listed it as Class III in its Enforcement Report dated Sep 24, 2025; distribution: Colorado, Illinois, Minnesota, Missouri, Utah.
Record status as published: Terminated (terminated Jan 6, 2026). openFDA data last updated Oct 21, 2026.
Have this product? Check FDA.gov and your retailer. This page reproduces an FDA Enforcement Report record and is not a public alert. Look for the firm's recall notice on the FDA's recalls page, or ask the store where you bought it what to do. If you think you got sick from a food, contact a health care provider.
Recall details
- Product
- 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.
- Product quantity
- 925 cases
- Reason for recall
- Goldband Snapper is recalled because testing confirmed fish is Sharptooth Snapper.
- Codes, lots and dates on the package
- Production date: 21824, 21924, 22124, and 22224.
- Distribution pattern
- Distributed in CO, IL, MO, MN and UT.
- Recalling firm
- E&E Foods Inc, Renton, WA
- Classification
- Class III — the FDA uses this class for a situation in which using or being exposed to the product is not likely to cause adverse health consequences.
- Voluntary or mandated
- Voluntary: Firm initiated
- How the firm first notified customers
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Dates
| Event | Date |
|---|---|
| Recall initiated by the firm | Sep 11, 2025 |
| Classified by the FDA | Sep 22, 2025 |
| Published in the Enforcement Report | Sep 24, 2025 |
| Terminated | Jan 6, 2026 |
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Sources
- U.S. Food and Drug Administration, openFDA food enforcement reports, recall number H-0620-2025 (openFDA record). Data provided by the U.S. Food and Drug Administration (https://open.fda.gov).
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