Dried Anchovy (Gobugi Holdings) – Botulinum Risk (2018)
Class II: A situation in which use of, or exposure to, a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote
Class II recall indicates potential for temporary health effects.
This AI-generated summary is provided for general informational purposes only and is derived from publicly available recall notices. It supplements but does not replace official agency classifications or safety instructions.
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
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
Brand
Gobugi Holdings Inc
Lot Codes / Batch Numbers
No codes
Products Sold
No codes
Gobugi Holdings Inc is recalling Dried Anchovy, size (S), (M), (L), packaged in 1.5 kg. cardboard box without brand name. The cardbo due to Product is uneviscerated and has the potential to be contaminated with Clostridium botulinum.. This is a Class I recall, indicating a high risk of serious health consequences. Based on FDA enforcement report.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Product is uneviscerated and has the potential to be contaminated with Clostridium botulinum.
Recommended Action
Per FDA guidance
Consumers should stop using the product and contact the recalling firm or return it to the place of purchase.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticeDistribution
As reported by FDA
CA, IN, OR
Page updated: Jan 6, 2026