Food Recall Check
Class II · Moderate risk Terminated Initiated Jan 12, 2018 (9 years ago)

Dried Anchovy recall

Recalled by Gobugi Holdings Inc · Beaverton, OR, United States

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

Product is uneviscerated and has the potential to be contaminated with Clostridium botulinum.

Pathogen: Botulism

Clostridium botulinum toxin, a risk in improperly canned or under-processed foods.

The most serious food recalls: a contaminated product can cause outbreaks, hospitalisations and deaths, especially for pregnant people, young children, older adults and anyone with a weakened immune system. All bacteria & viruses recalls.

What was recalled

Dried Anchovy, size (S), (M), (L), packaged in 1.5 kg. cardboard box without brand name. The cardboard box states "***IMPORTED BY: GOBUGI HOLDINGS, INC. 4520 SW 110TH AVE. BEAVERTON, OREGON 97005***PRODUCT OF REPUBLIC OF KOREA***". Small (S) Anchovy Korea, packaged in a clear plastic clam shell container, net wt. 9.6 oz. UPC 4 98900 00146 1. Medium (M) Anchovy Korea, packaged in a clear plastic clam shell container, net wt. 8.0 oz. UPC 4 98900 00149 2. Large (L) Anchovy Korea, packaged in a clear plastic clam shell container, net wt. 8.8 oz. UPC 4 98900 00148 5.

Quantity: 6000 cases (bulk); Unknown amount of retail containers

Food: Seafood & fish

Lot codes, dates and UPCs

A recall covers only these codes. Compare them with the lot number, best-by date or UPC printed on your package.

No codes

Where it was sold

California Oregon

FDA's distribution note: Distributed in California and Oregon

Check the codes, then return or discard. Class II means eating it may cause temporary or reversible health problems. If your package matches the recalled codes, do not eat it - return it to the store or throw it away. FDA lists this recall as terminated: the company has finished removing the product, so it should no longer be on shelves - but it can still be in a freezer or pantry.

Recalling firm
Gobugi Holdings Inc
Initiated by
Voluntary: Firm initiated
Recall initiated
Jan 12, 2018
In FDA report of
Feb 28, 2018
Terminated
Jul 27, 2018
FDA recall number
F-0828-2018 · event 78940
Official record
FDA enforcement report search

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